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    <title>Talking the Cure by Hogan Lovells Cadwalader</title>
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    <description><![CDATA[<p>Hogan Lovells Calwalader is always thinking about how to conquer and foresee the most significant industry issues facing our clients. Hear first-hand from our lawyers around the world on significant developments in the Life Sciences &amp; Health Care sector and why they are so passionate about the industry. We unpack new and exciting industry trends and bring you more outside perspectives to keep you ahead of the curve.</p>]]></description>
    <pubDate>Mon, 20 Oct 2025 19:21:56 +0200</pubDate>
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        <copyright>Copyright 2026. All rights reserved.</copyright>
    <category>Business</category>
    <ttl>1440</ttl>
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          <itunes:summary>Hogan Lovells is always thinking about how to conquer and foresee the most significant industry issues facing our clients. If you’ve been following us for the past two years, you’ve heard first-hand from our lawyers around the world on significant developments in the Life Sciences &amp;amp;amp; Health Care sector and why they are so passionate about the industry. In season 3, we’ll unpack new and exciting industry trends and bring you more outside perspectives to keep you ahead of the curve.</itunes:summary>
        <itunes:author>Hogan Lovells Cadwalader</itunes:author>
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        <itunes:name>Hogan Lovells Cadwalader</itunes:name>
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        <title>Talking the Cure by Hogan Lovells Cadwalader</title>
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        <title>It’s a Brave New World: Pharma ad/promo enforcement is changing in the U.S. and Europe, and companies should, too</title>
        <itunes:title>It’s a Brave New World: Pharma ad/promo enforcement is changing in the U.S. and Europe, and companies should, too</itunes:title>
        <link>https://talkingthecure.podbean.com/e/it-s-a-brave-new-world-pharma-adpromo-enforcement-is-changing-in-the-us-and-europe-and-companies-should-too/</link>
                    <comments>https://talkingthecure.podbean.com/e/it-s-a-brave-new-world-pharma-adpromo-enforcement-is-changing-in-the-us-and-europe-and-companies-should-too/#comments</comments>        <pubDate>Mon, 20 Oct 2025 19:21:56 +0200</pubDate>
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                                    <description><![CDATA[<p>FDA’s recent splash of 100+ enforcement letters objecting to drug advertising looks like a trend, not a blip.  And although the UK and EU prohibit DTC ads for Rx drugs, there are new efforts creating risk for pharma companies, even if they’re not the main focus.  In this episode of Talking the Cure, host Phil Katz is joined by Heidi Gertner, Sally Gu, and Bonella Ramsay to unpack what’s happening and what it means pharma companies should be thinking about, and steps they should be taking now to mitigate current – and future – risks. </p>
]]></description>
                                                            <content:encoded><![CDATA[<p>FDA’s recent splash of 100+ enforcement letters objecting to drug advertising looks like a trend, not a blip.  And although the UK and EU prohibit DTC ads for Rx drugs, there are new efforts creating risk for pharma companies, even if they’re not the main focus.  In this episode of Talking the Cure, host Phil Katz is joined by Heidi Gertner, Sally Gu, and Bonella Ramsay to unpack what’s happening and what it means pharma companies should be thinking about, and steps they should be taking now to mitigate current – and future – risks. </p>
]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[FDA’s recent splash of 100+ enforcement letters objecting to drug advertising looks like a trend, not a blip.  And although the UK and EU prohibit DTC ads for Rx drugs, there are new efforts creating risk for pharma companies, even if they’re not the main focus.  In this episode of Talking the Cure, host Phil Katz is joined by Heidi Gertner, Sally Gu, and Bonella Ramsay to unpack what’s happening and what it means pharma companies should be thinking about, and steps they should be taking now to mitigate current – and future – risks. ]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1581</itunes:duration>
                <itunes:episode>27</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>The future of drug pricing: IRA, MFN, and tariff pressures explained</title>
        <itunes:title>The future of drug pricing: IRA, MFN, and tariff pressures explained</itunes:title>
        <link>https://talkingthecure.podbean.com/e/the-future-of-drug-pricing-ira-mfn-and-tariff-pressures-explained/</link>
                    <comments>https://talkingthecure.podbean.com/e/the-future-of-drug-pricing-ira-mfn-and-tariff-pressures-explained/#comments</comments>        <pubDate>Mon, 22 Sep 2025 19:48:45 +0200</pubDate>
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                                    <description><![CDATA[<p>In this episode of Talking the Cure, Hogan Lovells partners Phil Katz, Alice Valder Curren, and Jane Summerfield discuss the evolving landscape of pharmaceutical pricing, particularly legislative and administrative changes in the United States and their implications in Europe. The discussion includes the Inflation Reduction Act (IRA) in the U.S., Most Favored Nations (MFN) pricing policies, and the impact of tariffs on drug prices and supply chains.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode of Talking the Cure, Hogan Lovells partners Phil Katz, Alice Valder Curren, and Jane Summerfield discuss the evolving landscape of pharmaceutical pricing, particularly legislative and administrative changes in the United States and their implications in Europe. The discussion includes the Inflation Reduction Act (IRA) in the U.S., Most Favored Nations (MFN) pricing policies, and the impact of tariffs on drug prices and supply chains.</p>
]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[In this episode of Talking the Cure, Hogan Lovells partners Phil Katz, Alice Valder Curren, and Jane Summerfield discuss the evolving landscape of pharmaceutical pricing, particularly legislative and administrative changes in the United States and their implications in Europe. The discussion includes the Inflation Reduction Act (IRA) in the U.S., Most Favored Nations (MFN) pricing policies, and the impact of tariffs on drug prices and supply chains.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1278</itunes:duration>
                <itunes:episode>26</itunes:episode>
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    <item>
        <title>AI at the crossroads: Global developments shaping life sciences</title>
        <itunes:title>AI at the crossroads: Global developments shaping life sciences</itunes:title>
        <link>https://talkingthecure.podbean.com/e/ai-at-the-crossroads-global-developments-shaping-life-sciences/</link>
                    <comments>https://talkingthecure.podbean.com/e/ai-at-the-crossroads-global-developments-shaping-life-sciences/#comments</comments>        <pubDate>Tue, 29 Jul 2025 17:28:39 +0200</pubDate>
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                                    <description><![CDATA[<p>In this episode of Talking the Cure, Hogan Lovells partners Phil Katz, Melissa Bianchi, and Jodi Scott explore how artificial intelligence is transforming the pharmaceutical, biotech, and medical device industries. From AI-driven clinical trials and diagnostic tools to regulatory challenges and global compliance complexities, the discussion dives deep into both the promise and the pitfalls of integrating AI in health care. Tune in to hear how industry leaders are navigating this fast-evolving space – and what companies need to know to stay ahead.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode of Talking the Cure, Hogan Lovells partners Phil Katz, Melissa Bianchi, and Jodi Scott explore how artificial intelligence is transforming the pharmaceutical, biotech, and medical device industries. From AI-driven clinical trials and diagnostic tools to regulatory challenges and global compliance complexities, the discussion dives deep into both the promise and the pitfalls of integrating AI in health care. Tune in to hear how industry leaders are navigating this fast-evolving space – and what companies need to know to stay ahead.</p>
]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[In this episode of Talking the Cure, Hogan Lovells partners Phil Katz, Melissa Bianchi, and Jodi Scott explore how artificial intelligence is transforming the pharmaceutical, biotech, and medical device industries. From AI-driven clinical trials and diagnostic tools to regulatory challenges and global compliance complexities, the discussion dives deep into both the promise and the pitfalls of integrating AI in health care. Tune in to hear how industry leaders are navigating this fast-evolving space – and what companies need to know to stay ahead.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1644</itunes:duration>
                <itunes:episode>25</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Planning the Pivot: Onshoring Pharma/Biotech Manufacturing in a Brave New World</title>
        <itunes:title>Planning the Pivot: Onshoring Pharma/Biotech Manufacturing in a Brave New World</itunes:title>
        <link>https://talkingthecure.podbean.com/e/planning-the-pivot-onshoring-pharmabiotech-manufacturing-in-a-brave-new-world/</link>
                    <comments>https://talkingthecure.podbean.com/e/planning-the-pivot-onshoring-pharmabiotech-manufacturing-in-a-brave-new-world/#comments</comments>        <pubDate>Mon, 09 Jun 2025 10:33:28 +0200</pubDate>
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                                    <description><![CDATA[<p>Starting with tariffs and Executive Orders, there are myriad incentives – some would say imperatives – for pharma and biotech companies to increase and expand manufacturing in the US.  But this is a classic “easier said than done” situation, for a number of reasons.  Sally Gu and Chris Middendorf, drug manufacturing and quality experts and leading members of the Hogan Lovells Pharma/Biotech Regulatory Compliance and Enforcement Practice, join Phil Katz to dive into one particular set of issues – those related to the technical, logistical and other practical considerations of manufacturing these products.  Drawing on their years of experience advising and advocating for product sponsors, manufacturers, and others on how to efficiently and compliantly manufacture or source drug and biotechnology products, Sally and Chris tackle the challenges in adding or changing manufacturing sites.  They bring an integrated and strategic approach, and discuss how companies can (and should) do the same.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>Starting with tariffs and Executive Orders, there are myriad incentives – some would say imperatives – for pharma and biotech companies to increase and expand manufacturing in the US.  But this is a classic “easier said than done” situation, for a number of reasons.  Sally Gu and Chris Middendorf, drug manufacturing and quality experts and leading members of the Hogan Lovells Pharma/Biotech Regulatory Compliance and Enforcement Practice, join Phil Katz to dive into one particular set of issues – those related to the technical, logistical and other practical considerations of manufacturing these products.  Drawing on their years of experience advising and advocating for product sponsors, manufacturers, and others on how to efficiently and compliantly manufacture or source drug and biotechnology products, Sally and Chris tackle the challenges in adding or changing manufacturing sites.  They bring an integrated and strategic approach, and discuss how companies can (and should) do the same.</p>
]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[Starting with tariffs and Executive Orders, there are myriad incentives – some would say imperatives – for pharma and biotech companies to increase and expand manufacturing in the US.  But this is a classic “easier said than done” situation, for a number of reasons.  Sally Gu and Chris Middendorf, drug manufacturing and quality experts and leading members of the Hogan Lovells Pharma/Biotech Regulatory Compliance and Enforcement Practice, join Phil Katz to dive into one particular set of issues – those related to the technical, logistical and other practical considerations of manufacturing these products.  Drawing on their years of experience advising and advocating for product sponsors, manufacturers, and others on how to efficiently and compliantly manufacture or source drug and biotechnology products, Sally and Chris tackle the challenges in adding or changing manufacturing sites.  They bring an integrated and strategic approach, and discuss how companies can (and should) do the same.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1749</itunes:duration>
                <itunes:episode>24</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>A cure worse than the disease?  Using tariffs to bolster U.S. pharma manufacturing</title>
        <itunes:title>A cure worse than the disease?  Using tariffs to bolster U.S. pharma manufacturing</itunes:title>
        <link>https://talkingthecure.podbean.com/e/a-cure-worse-than-the-disease%c2%a0-using-tariffs-to-bolster-us-pharma-manufacturing/</link>
                    <comments>https://talkingthecure.podbean.com/e/a-cure-worse-than-the-disease%c2%a0-using-tariffs-to-bolster-us-pharma-manufacturing/#comments</comments>        <pubDate>Fri, 09 May 2025 18:35:34 +0200</pubDate>
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                                    <description><![CDATA[<p>In this episode of Talking the Cure, Phil Katz talks with Cybil Roehrenbeck, Josh Gelula, and Kelly Zhang about the announced and seemingly ever-changing plans for tariffs on imported goods – and pharmaceutical products in particular – may effect the industry, as well as the availability and cost of drugs.  The discussion unpacks the law, the politics, and policy to offer suggestions on steps businesses can be taking to deal with the impacts.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode of Talking the Cure, Phil Katz talks with Cybil Roehrenbeck, Josh Gelula, and Kelly Zhang about the announced and seemingly ever-changing plans for tariffs on imported goods – and pharmaceutical products in particular – may effect the industry, as well as the availability and cost of drugs.  The discussion unpacks the law, the politics, and policy to offer suggestions on steps businesses can be taking to deal with the impacts.</p>
]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/yibsnny9e9bghpec/TTC_Tariffs6by2z.mp3" length="66971857" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode of Talking the Cure, Phil Katz talks with Cybil Roehrenbeck, Josh Gelula, and Kelly Zhang about the announced and seemingly ever-changing plans for tariffs on imported goods – and pharmaceutical products in particular – may effect the industry, as well as the availability and cost of drugs.  The discussion unpacks the law, the politics, and policy to offer suggestions on steps businesses can be taking to deal with the impacts.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1674</itunes:duration>
                <itunes:episode>23</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Pharma – The Last Word  – Breaking Barriers: The FDA’s Evolving Approach to Biosimilars and Interchangeability</title>
        <itunes:title>Pharma – The Last Word  – Breaking Barriers: The FDA’s Evolving Approach to Biosimilars and Interchangeability</itunes:title>
        <link>https://talkingthecure.podbean.com/e/pharma-the-last-word-breaking-barriers-the-fda-s-evolving-approach-to-biosimilars-and-interchangeability/</link>
                    <comments>https://talkingthecure.podbean.com/e/pharma-the-last-word-breaking-barriers-the-fda-s-evolving-approach-to-biosimilars-and-interchangeability/#comments</comments>        <pubDate>Wed, 25 Sep 2024 07:41:53 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/4773c391-b375-37f7-9a13-2d5c544345e5</guid>
                                    <description><![CDATA[<p>In this episode, host <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a> sits down with <a href='https://www.hoganlovells.com/en/cho-deborah'>Deborah Cho</a>, to discuss the evolving landscape of biosimilarity and interchangeability. They dive into the FDA's changing approach, highlighting the shift towards treating biosimilars and interchangeable biosimilars as a single category. Deborah explains how advancements in technology and experience have reduced the need for additional studies, and why the FDA is pushing for a statutory change to streamline approvals. </p>
<p>The future episodes will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode, host <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a> sits down with <a href='https://www.hoganlovells.com/en/cho-deborah'>Deborah Cho</a>, to discuss the evolving landscape of biosimilarity and interchangeability. They dive into the FDA's changing approach, highlighting the shift towards treating biosimilars and interchangeable biosimilars as a single category. Deborah explains how advancements in technology and experience have reduced the need for additional studies, and why the FDA is pushing for a statutory change to streamline approvals. </p>
<p>The future episodes will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></content:encoded>
                                    
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                <itunes:summary>In this episode, host Phil Katz sits down with Deborah Cho, a legal expert in biologics and biosimilars, to discuss the evolving landscape of biosimilarity and interchangeability. They dive into the FDA’s changing approach, highlighting the shift towards treating biosimilars and interchangeable biosimilars as a single category. Deborah explains how advancements in technology and experience have reduced the need for additional studies, and why the FDA is pushing for a statutory change to streamline approvals.</itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1348</itunes:duration>
                <itunes:episode>22</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Drafting the Future: Unpacking the FDA's Clinical Trial Diversity Action Plan</title>
        <itunes:title>Drafting the Future: Unpacking the FDA's Clinical Trial Diversity Action Plan</itunes:title>
        <link>https://talkingthecure.podbean.com/e/drafting-the-future-unpacking-the-fdas-clinical-trial-diversity-action-plan/</link>
                    <comments>https://talkingthecure.podbean.com/e/drafting-the-future-unpacking-the-fdas-clinical-trial-diversity-action-plan/#comments</comments>        <pubDate>Fri, 12 Jul 2024 06:00:00 +0200</pubDate>
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                                    <description><![CDATA[<p>In the third part of our clinical trial diversity series, <a href='https://www.hoganlovells.com/en/cho-deborah'>Deborah Cho</a>, <a href='https://www.hoganlovells.com/en/agu-stephanie'>Stephanie Agu</a>, and <a href='https://www.hoganlovells.com/en/grey-ashley'>Ashley Grey</a> dissect FDA's new draft guidance on Diversity Action Plans for clinical trials, released on June 28, 2024. Discover what this pivotal document means for clinical trial design and conduct, and its implications for drug and biologic sponsors. Tune in for an insightful discussion on the future of clinical trials and FDA recommendations to ensure diverse participant inclusion.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In the third part of our clinical trial diversity series, <a href='https://www.hoganlovells.com/en/cho-deborah'>Deborah Cho</a>, <a href='https://www.hoganlovells.com/en/agu-stephanie'>Stephanie Agu</a>, and <a href='https://www.hoganlovells.com/en/grey-ashley'>Ashley Grey</a> dissect FDA's new draft guidance on Diversity Action Plans for clinical trials, released on June 28, 2024. Discover what this pivotal document means for clinical trial design and conduct, and its implications for drug and biologic sponsors. Tune in for an insightful discussion on the future of clinical trials and FDA recommendations to ensure diverse participant inclusion.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></content:encoded>
                                    
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                <itunes:summary>In this episode of the third part of the clinical trial diversity series, Ashley Gray, Deborah Chow and Stephanie Agu dissect the FDA’s new draft guidance on the Clinical Trial Diversity Action Plan, released on June 28, 2024. Discover how this pivotal document influences clinical trial design and conduct, thoroughly exploring its implications for drug and biologic sponsors. Tune in for an insightful discussion on the future of clinical trials and the strategies to ensure diverse and effective participant inclusion.</itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>843</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>6</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Pharma – The Last Word – Early Access Unlocked, navigating EU programs for pre-approval drug access</title>
        <itunes:title>Pharma – The Last Word – Early Access Unlocked, navigating EU programs for pre-approval drug access</itunes:title>
        <link>https://talkingthecure.podbean.com/e/pharma-the-last-word-early-access-unlocked-navigating-eu-programs-for-pre-approval-drug-access/</link>
                    <comments>https://talkingthecure.podbean.com/e/pharma-the-last-word-early-access-unlocked-navigating-eu-programs-for-pre-approval-drug-access/#comments</comments>        <pubDate>Fri, 28 Jun 2024 11:29:12 +0200</pubDate>
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                                    <description><![CDATA[<p>In this episode <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a> and <a href='https://www.hoganlovells.com/en/hein-van-den-bos'>Hein van den Bos </a>discuss early access programs in the EU, exploring the various types of programs, their practical implications, and the regulatory challenges. They delve into compassionate use programs, named patient supply, and the nuances of implementing these programs across different EU countries. The conversation also touches on the benefits and risks of early access, including potential ethical and reputational concerns.</p>
<p>The future episodes will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a> and <a href='https://www.hoganlovells.com/en/hein-van-den-bos'>Hein van den Bos </a>discuss early access programs in the EU, exploring the various types of programs, their practical implications, and the regulatory challenges. They delve into compassionate use programs, named patient supply, and the nuances of implementing these programs across different EU countries. The conversation also touches on the benefits and risks of early access, including potential ethical and reputational concerns.</p>
<p>The future episodes will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[In this episode Phil Katz and Hein van den Bos discuss early access programs in the EU, exploring the various types of programs, their practical implications, and the regulatory challenges. They delve into compassionate use programs, named patient supply, and the nuances of implementing these programs across different EU countries. The conversation also touches on the benefits and risks of early access, including potential ethical and reputational concerns.
The future episodes will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.
You can find additional thought leadership and information regarding digital health on Engage.
If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠ and ⁠⁠⁠⁠Twitter⁠⁠⁠⁠.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1060</itunes:duration>
                <itunes:episode>21</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Pharma – The Last Word – Regulatory and legal trends in the pharma and biotech industries</title>
        <itunes:title>Pharma – The Last Word – Regulatory and legal trends in the pharma and biotech industries</itunes:title>
        <link>https://talkingthecure.podbean.com/e/pharma-the-last-word-the-inaugural-episode-1717150210/</link>
                    <comments>https://talkingthecure.podbean.com/e/pharma-the-last-word-the-inaugural-episode-1717150210/#comments</comments>        <pubDate>Fri, 31 May 2024 12:10:10 +0200</pubDate>
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                                    <description><![CDATA[<p>In this episode host <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a>, discusses regulatory and legal trends in the pharma and biotech industries with <a href='https://www.hoganlovells.com/en/komal-a-karnik'>Komal Karnik Nigam</a>. They delve into the FDA's evolving approach to data packages required for drug approval, highlighting the increased flexibility in accepting alternative forms of evidence. Komal explains how FDA's guidance has shifted from demanding large, multicenter trials to considering confirmatory evidence such as natural history studies, mechanistic data, and data from other products in the same class. The episode emphasizes the importance of strategic planning and early consideration of data presentation in regulatory interactions.</p>
<p>The future episodes will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode host <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a>, discusses regulatory and legal trends in the pharma and biotech industries with <a href='https://www.hoganlovells.com/en/komal-a-karnik'>Komal Karnik Nigam</a>. They delve into the FDA's evolving approach to data packages required for drug approval, highlighting the increased flexibility in accepting alternative forms of evidence. Komal explains how FDA's guidance has shifted from demanding large, multicenter trials to considering confirmatory evidence such as natural history studies, mechanistic data, and data from other products in the same class. The episode emphasizes the importance of strategic planning and early consideration of data presentation in regulatory interactions.</p>
<p>The future episodes will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
]]></content:encoded>
                                    
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                <itunes:summary>In this episode of ”Pharma - The last word,” host Phil Katz, discusses regulatory and legal trends in the pharma and biotech industries with Komal Karnik Nigam. They delve into the FDA’s evolving approach to data packages required for drug approval, highlighting the increased flexibility in accepting alternative forms of evidence. Komal explains how FDA’s guidance has shifted from demanding large, multicenter trials to considering confirmatory evidence such as natural history studies, mechanistic data, and data from other products in the same class. The episode emphasizes the importance of strategic planning and early consideration of data presentation in regulatory interactions.</itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
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        <itunes:season>5</itunes:season>
        <itunes:episode>2</itunes:episode>
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    <item>
        <title>Pharma – The Last Word - The inaugural episode</title>
        <itunes:title>Pharma – The Last Word - The inaugural episode</itunes:title>
        <link>https://talkingthecure.podbean.com/e/pharma-the-last-word-the-inaugural-episode/</link>
                    <comments>https://talkingthecure.podbean.com/e/pharma-the-last-word-the-inaugural-episode/#comments</comments>        <pubDate>Mon, 29 Apr 2024 21:33:37 +0200</pubDate>
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                                    <description><![CDATA[<p>Welcome to the inaugural episode of "Pharma – The Last Word", a podcast hosted by Partner <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a> from <a href='https://www.hoganlovells.com/en'>Hogan Lovells</a>. This series aims to dive into the intricate world of pharmaceuticals and biotech regulatory and legal landscapes, exploring new innovations, trends, and their practical impacts. Join Phil and his first guest, <a href='https://www.hoganlovells.com/en/lynn-mehler'>Lynn Mehler</a>, co-head of the <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>Life Sciences and Health Care industry sector</a>, and Lead of the Pharmaceuticals and Biotech Regulatory Practice, as they discuss the unique insights and deep expertise their team brings to the table, the largest of its kind outside the FDA. They will share the inner workings of their practice, how they stay ahead of industry trends, and their passion for the field.</p>
<p>Each episode will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
<p> </p>
]]></description>
                                                            <content:encoded><![CDATA[<p>Welcome to the inaugural episode of "Pharma – The Last Word", a podcast hosted by Partner <a href='https://www.hoganlovells.com/en/philip-katz'>Phil Katz</a> from <a href='https://www.hoganlovells.com/en'>Hogan Lovells</a>. This series aims to dive into the intricate world of pharmaceuticals and biotech regulatory and legal landscapes, exploring new innovations, trends, and their practical impacts. Join Phil and his first guest, <a href='https://www.hoganlovells.com/en/lynn-mehler'>Lynn Mehler</a>, co-head of the <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>Life Sciences and Health Care industry sector</a>, and Lead of the Pharmaceuticals and Biotech Regulatory Practice, as they discuss the unique insights and deep expertise their team brings to the table, the largest of its kind outside the FDA. They will share the inner workings of their practice, how they stay ahead of industry trends, and their passion for the field.</p>
<p>Each episode will focus on specific areas of the law, such as drug development, clinical trials, FDA compliance, and more, providing listeners with a detailed look at the complexities of pharmaceutical regulations and practical strategies for navigating them.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.</p>
<p> </p>
]]></content:encoded>
                                    
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                <itunes:summary>A podcast hosted by Partner Phil Katz from Hogan Lovells. This series aims to dive into the intricate world of pharmaceuticals and biotech regulatory and legal landscapes, exploring new innovations, trends, and their practical impacts. Join Phil and his first guest, Lynn Mehler, co-head of the Life Sciences and Health Care industry sector, and Lead of the Pharmaceuticals and Biotech Regulatory Practice, as they discuss the unique insights and deep expertise their team brings to the table, the largest of its kind outside the FDA. They will share the inner workings of their practice, how they stay ahead of industry trends, and their passion for the field.</itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>457</itunes:duration>
        <itunes:season>5</itunes:season>
        <itunes:episode>1</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Securing the Crown Jewels: Navigating IP and cybersecurity in the life science industry</title>
        <itunes:title>Securing the Crown Jewels: Navigating IP and cybersecurity in the life science industry</itunes:title>
        <link>https://talkingthecure.podbean.com/e/securing-the-crown-jewels-navigating-ip-and-cybersecurity-in-the-life-science-industry/</link>
                    <comments>https://talkingthecure.podbean.com/e/securing-the-crown-jewels-navigating-ip-and-cybersecurity-in-the-life-science-industry/#comments</comments>        <pubDate>Thu, 11 Apr 2024 09:09:00 +0200</pubDate>
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                                    <description><![CDATA[<p>In this episode of Talking the Cure Hogan Lovells Life Sciences and Health Care Podcast <a href='https://www.hoganlovells.com/en/ruud-vandervelden'>Ruud van der Velden </a>and <a href='https://www.hoganlovells.com/en/van-dam-chantal'>Chantal Van Dam</a> highlight the importance of protecting intellectual property and trade secrets in the life sciences and health care industry. They discuss the legal framework for trade secrets in the EU, the increasing focus of cybercriminals on valuable company data beyond personal information, and provide key recommendations for companies to safeguard their most critical assets against theft and unauthorized disclosure.</p>
<p>
You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>
If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.



</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode of Talking the Cure Hogan Lovells Life Sciences and Health Care Podcast <a href='https://www.hoganlovells.com/en/ruud-vandervelden'>Ruud van der Velden </a>and <a href='https://www.hoganlovells.com/en/van-dam-chantal'>Chantal Van Dam</a> highlight the importance of protecting intellectual property and trade secrets in the life sciences and health care industry. They discuss the legal framework for trade secrets in the EU, the increasing focus of cybercriminals on valuable company data beyond personal information, and provide key recommendations for companies to safeguard their most critical assets against theft and unauthorized disclosure.</p>
<p>
You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/Home'>Engage</a>.</p>
<p>
If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠<a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn⁠⁠⁠⁠ </a>and ⁠⁠⁠⁠<a href='https://twitter.com/HLLifeSciences'>Twitter⁠⁠⁠⁠</a>.



</p>
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                <itunes:summary><![CDATA[In this episode of Talking the Cure Hogan Lovells Life Sciences and Health Care Podcast Ruud van der Velden and Chantal Van Dam highlight the importance of protecting intellectual property and trade secrets in the life sciences and health care industry. They discuss the legal framework for trade secrets in the EU, the increasing focus of cybercriminals on valuable company data beyond personal information, and provide key recommendations for companies to safeguard their most critical assets against theft and unauthorized disclosure.

You can find additional thought leadership and information regarding digital health on Engage.

If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠ and ⁠⁠⁠⁠Twitter⁠⁠⁠⁠.



]]></itunes:summary>
        <itunes:author>Hogan Lovells Cadwalader</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1947</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>5</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Discussing UK medical device regulations</title>
        <itunes:title>Discussing UK medical device regulations</itunes:title>
        <link>https://talkingthecure.podbean.com/e/discussing-uk-medical-device-regulations/</link>
                    <comments>https://talkingthecure.podbean.com/e/discussing-uk-medical-device-regulations/#comments</comments>        <pubDate>Thu, 21 Mar 2024 14:15:00 +0100</pubDate>
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                                    <description><![CDATA[In this episode Jane Summerfield and Owen Robinson discuss UK medical device regulation, focusing on the regulatory roadmap published by the MHRA, its implications for businesses, and the process for legislation development. They highlight the delay in core regulation target dates, the importance of stakeholder consultations, and the potential impacts of the upcoming general election on the roadmap's timeline and policy direction.
You can find additional thought leadership and information regarding digital health on ⁠⁠⁠⁠HL Engage⁠⁠⁠⁠.
If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠ and ⁠⁠⁠⁠Twitter⁠⁠⁠⁠.]]></description>
                                                            <content:encoded><![CDATA[In this episode Jane Summerfield and Owen Robinson discuss UK medical device regulation, focusing on the regulatory roadmap published by the MHRA, its implications for businesses, and the process for legislation development. They highlight the delay in core regulation target dates, the importance of stakeholder consultations, and the potential impacts of the upcoming general election on the roadmap's timeline and policy direction.
You can find additional thought leadership and information regarding digital health on ⁠⁠⁠⁠HL Engage⁠⁠⁠⁠.
If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠ and ⁠⁠⁠⁠Twitter⁠⁠⁠⁠.]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[In this episode Jane Summerfield and Owen Robinson discuss UK medical device regulation, focusing on the regulatory roadmap published by the MHRA, its implications for businesses, and the process for legislation development. They highlight the delay in core regulation target dates, the importance of stakeholder consultations, and the potential impacts of the upcoming general election on the roadmap's timeline and policy direction.
You can find additional thought leadership and information regarding digital health on ⁠⁠⁠⁠HL Engage⁠⁠⁠⁠.
If you are interested in more information about Life Sciences and Health Care, follow us via ⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠ and ⁠⁠⁠⁠Twitter⁠⁠⁠⁠.]]></itunes:summary>
        <itunes:author>Hogan Lovells Cadwalader</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1027</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>4</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking the Cure - Exploring the industry with Richard Backhaus and Lars Cornels (Drägerwerk AG &amp; Co. KGaA) - Part 2</title>
        <itunes:title>Talking the Cure - Exploring the industry with Richard Backhaus and Lars Cornels (Drägerwerk AG &amp; Co. KGaA) - Part 2</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-richard-backhaus-and-lars-cornels-dragerwerk-ag-co-kgaa-part-2/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-richard-backhaus-and-lars-cornels-dragerwerk-ag-co-kgaa-part-2/#comments</comments>        <pubDate>Thu, 29 Feb 2024 08:00:00 +0100</pubDate>
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                                    <description><![CDATA[<p>In the second part of the episode, <a href='https://www.hoganlovells.com/en/arne-thiermann'>⁠⁠Arne Thiermann⁠⁠</a> is leading the conversation with <a href='https://www.linkedin.com/in/richard-backhaus-a1a78277/'>⁠⁠Richard Backhaus⁠⁠</a>, and <a href='https://www.linkedin.com/in/lars-c-cornels-8bab9ba7/'>⁠⁠Lars Cornels⁠⁠</a> discussing the integration and implications of digital health, artificial intelligence, and legal considerations in the medical device industry. They explore how traditional companies like <a href='https://www.draeger.com/de_de/Home'>⁠⁠Drägerwerk AG &amp; Co. KGaA⁠⁠</a> adapt to digital innovation, the role of AI and software in life sciences, and the challenges and opportunities presented by regulatory environments. They delve into specific legal frameworks, such as the European Union's data strategy and the AI Act, discussing their impact on innovation and data access. The conversation also touches on the practical use of AI in legal work, the future of the profession, and the broader implications of AI on society and human behavior.</p>
<p>
</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/LoginRequiredPage.action'>⁠⁠⁠HL Engage⁠⁠⁠</a>.</p>
<p>If you are interested in more information all around Life Sciences and Health Care, follow us on <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>⁠⁠⁠LinkedIn⁠⁠⁠</a> and <a href='https://twitter.com/hllifesciences?lang=de'>⁠⁠⁠Twitter⁠⁠⁠</a>.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In the second part of the episode, <a href='https://www.hoganlovells.com/en/arne-thiermann'>⁠⁠Arne Thiermann⁠⁠</a> is leading the conversation with <a href='https://www.linkedin.com/in/richard-backhaus-a1a78277/'>⁠⁠Richard Backhaus⁠⁠</a>, and <a href='https://www.linkedin.com/in/lars-c-cornels-8bab9ba7/'>⁠⁠Lars Cornels⁠⁠</a> discussing the integration and implications of digital health, artificial intelligence, and legal considerations in the medical device industry. They explore how traditional companies like <a href='https://www.draeger.com/de_de/Home'>⁠⁠Drägerwerk AG &amp; Co. KGaA⁠⁠</a> adapt to digital innovation, the role of AI and software in life sciences, and the challenges and opportunities presented by regulatory environments. They delve into specific legal frameworks, such as the European Union's data strategy and the AI Act, discussing their impact on innovation and data access. The conversation also touches on the practical use of AI in legal work, the future of the profession, and the broader implications of AI on society and human behavior.</p>
<p><br>
</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/LoginRequiredPage.action'>⁠⁠⁠HL Engage⁠⁠⁠</a>.</p>
<p>If you are interested in more information all around Life Sciences and Health Care, follow us on <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>⁠⁠⁠LinkedIn⁠⁠⁠</a> and <a href='https://twitter.com/hllifesciences?lang=de'>⁠⁠⁠Twitter⁠⁠⁠</a>.</p>
]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[In the second part of the episode, ⁠⁠Arne Thiermann⁠⁠ is leading the conversation with ⁠⁠Richard Backhaus⁠⁠, and ⁠⁠Lars Cornels⁠⁠ discussing the integration and implications of digital health, artificial intelligence, and legal considerations in the medical device industry. They explore how traditional companies like ⁠⁠Drägerwerk AG &amp; Co. KGaA⁠⁠ adapt to digital innovation, the role of AI and software in life sciences, and the challenges and opportunities presented by regulatory environments. They delve into specific legal frameworks, such as the European Union's data strategy and the AI Act, discussing their impact on innovation and data access. The conversation also touches on the practical use of AI in legal work, the future of the profession, and the broader implications of AI on society and human behavior.

You can find additional thought leadership and information regarding digital health on ⁠⁠⁠HL Engage⁠⁠⁠.
If you are interested in more information all around Life Sciences and Health Care, follow us on ⁠⁠⁠LinkedIn⁠⁠⁠ and ⁠⁠⁠Twitter⁠⁠⁠.]]></itunes:summary>
        <itunes:author>Hogan Lovells Cadwalader</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1639</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>3</itunes:episode>
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    <item>
        <title>Talking the Cure - Exploring the industry with Richard Backhaus and Lars Cornels (Drägerwerk AG &amp; Co. KGaA) - Part 1</title>
        <itunes:title>Talking the Cure - Exploring the industry with Richard Backhaus and Lars Cornels (Drägerwerk AG &amp; Co. KGaA) - Part 1</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-richard-backhaus-and-lars-cornels-dragerwerk-ag-co-kgaa-part-1/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-richard-backhaus-and-lars-cornels-dragerwerk-ag-co-kgaa-part-1/#comments</comments>        <pubDate>Mon, 12 Feb 2024 08:00:00 +0100</pubDate>
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                                    <description><![CDATA[<p>In this first part of the episode, <a href='https://www.hoganlovells.com/en/arne-thiermann'>Arne Thiermann</a> is leading the conversation with <a href='https://www.linkedin.com/in/richard-backhaus-a1a78277/'>Richard Backhaus</a>, and <a href='https://www.linkedin.com/in/lars-c-cornels-8bab9ba7/'>Lars Cornels</a> discussing the integration and implications of digital health, artificial intelligence, and legal considerations in the medical device industry. They explore how traditional companies like <a href='https://www.draeger.com/de_de/Home'>Drägerwerk AG &amp; Co. KGaA</a> adapt to digital innovation, the role of AI and software in life sciences, and the challenges and opportunities presented by regulatory environments. They delve into specific legal frameworks, such as the European Union's data strategy and the AI Act, discussing their impact on innovation and data access. The conversation also touches on the practical use of AI in legal work, the future of the profession, and the broader implications of AI on society and human behavior.</p>
<p>
</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/LoginRequiredPage.action'>⁠HL Engage⁠</a>.</p>
<p>If you are interested in more information all around Life Sciences and Health Care, follow us on <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>⁠LinkedIn⁠</a> and <a href='https://twitter.com/hllifesciences?lang=de'>⁠Twitter⁠</a>.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this first part of the episode, <a href='https://www.hoganlovells.com/en/arne-thiermann'>Arne Thiermann</a> is leading the conversation with <a href='https://www.linkedin.com/in/richard-backhaus-a1a78277/'>Richard Backhaus</a>, and <a href='https://www.linkedin.com/in/lars-c-cornels-8bab9ba7/'>Lars Cornels</a> discussing the integration and implications of digital health, artificial intelligence, and legal considerations in the medical device industry. They explore how traditional companies like <a href='https://www.draeger.com/de_de/Home'>Drägerwerk AG &amp; Co. KGaA</a> adapt to digital innovation, the role of AI and software in life sciences, and the challenges and opportunities presented by regulatory environments. They delve into specific legal frameworks, such as the European Union's data strategy and the AI Act, discussing their impact on innovation and data access. The conversation also touches on the practical use of AI in legal work, the future of the profession, and the broader implications of AI on society and human behavior.</p>
<p><br>
</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/LoginRequiredPage.action'>⁠HL Engage⁠</a>.</p>
<p>If you are interested in more information all around Life Sciences and Health Care, follow us on <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>⁠LinkedIn⁠</a> and <a href='https://twitter.com/hllifesciences?lang=de'>⁠Twitter⁠</a>.</p>
]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/1603gzhq5sn8h8br/s_eef10010_podcast_play_82541691_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2024-1-11_2Fe3bda198-ab30-b6ac-c318-b6de3de36e17.mp3" length="70583944" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this first part of the episode, Arne Thiermann is leading the conversation with Richard Backhaus, and Lars Cornels discussing the integration and implications of digital health, artificial intelligence, and legal considerations in the medical device industry. They explore how traditional companies like Drägerwerk AG &amp; Co. KGaA adapt to digital innovation, the role of AI and software in life sciences, and the challenges and opportunities presented by regulatory environments. They delve into specific legal frameworks, such as the European Union's data strategy and the AI Act, discussing their impact on innovation and data access. The conversation also touches on the practical use of AI in legal work, the future of the profession, and the broader implications of AI on society and human behavior.

You can find additional thought leadership and information regarding digital health on ⁠HL Engage⁠.
If you are interested in more information all around Life Sciences and Health Care, follow us on ⁠LinkedIn⁠ and ⁠Twitter⁠.]]></itunes:summary>
        <itunes:author>Hogan Lovells Cadwalader</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1764</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>2</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking the Cure - Exploring the industry with Robert F. Church</title>
        <itunes:title>Talking the Cure - Exploring the industry with Robert F. Church</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-robert-f-church/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-robert-f-church/#comments</comments>        <pubDate>Wed, 24 Jan 2024 11:33:00 +0100</pubDate>
        <guid isPermaLink="false">899202a5-2a4d-484b-821b-aa098468018e</guid>
                                    <description><![CDATA[<p>In this episode, <a href='https://www.hoganlovells.com/en/robert-church'>Robert F. Church⁠</a> takes the time to look back on his career with us. We talk about what ultimately led him to become a lawyer, how he ended up at Hogan Lovells, and how he became the institution in clinical trials. Of course, we also talk about what it means to manage such a heavy workload, how he takes time to switch off, and what he would like to pass on to aspiring colleagues who would like to pursue a career in this field.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/LoginRequiredPage.action'>HL Engage</a>.</p>
<p>If you are interested in more information all around Life Sciences and Health Care, follow us on <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn</a> and <a href='https://twitter.com/hllifesciences?lang=de'>Twitter</a>.</p>
]]></description>
                                                            <content:encoded><![CDATA[<p>In this episode, <a href='https://www.hoganlovells.com/en/robert-church'>Robert F. Church⁠</a> takes the time to look back on his career with us. We talk about what ultimately led him to become a lawyer, how he ended up at Hogan Lovells, and how he became the institution in clinical trials. Of course, we also talk about what it means to manage such a heavy workload, how he takes time to switch off, and what he would like to pass on to aspiring colleagues who would like to pursue a career in this field.</p>
<p>You can find additional thought leadership and information regarding digital health on <a href='https://www.engage.hoganlovells.com/knowledgeservices/LoginRequiredPage.action'>HL Engage</a>.</p>
<p>If you are interested in more information all around Life Sciences and Health Care, follow us on <a href='https://www.linkedin.com/showcase/hogan-lovells-life-sciences'>LinkedIn</a> and <a href='https://twitter.com/hllifesciences?lang=de'>Twitter</a>.</p>
]]></content:encoded>
                                    
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                <itunes:summary><![CDATA[In this episode, Robert F. Church⁠ takes the time to look back on his career with us. We talk about what ultimately led him to become a lawyer, how he ended up at Hogan Lovells, and how he became the institution in clinical trials. Of course, we also talk about what it means to manage such a heavy workload, how he takes time to switch off, and what he would like to pass on to aspiring colleagues who would like to pursue a career in this field.
You can find additional thought leadership and information regarding digital health on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells Cadwalader</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2190</itunes:duration>
        <itunes:season>5</itunes:season>
        <itunes:episode>1</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking the Cure - Exploring the industry with Alice Valder Curran</title>
        <itunes:title>Talking the Cure - Exploring the industry with Alice Valder Curran</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-alice-valder-curran/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-alice-valder-curran/#comments</comments>        <pubDate>Thu, 16 Nov 2023 13:13:00 +0100</pubDate>
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                                    <description><![CDATA[In this episode, Alice Valder Curran sits down with us to talk about her impressive career, why she ultimately chose Hogan Lovells as her employer, and what it takes to be successful in this area of the industry, even in times when you can only work part-time. Alice gives us a behind-the-scenes look at how to create your own niche and surround yourself with people who have the same standards for themselves and the same sense of quality.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Alice Valder Curran sits down with us to talk about her impressive career, why she ultimately chose Hogan Lovells as her employer, and what it takes to be successful in this area of the industry, even in times when you can only work part-time. Alice gives us a behind-the-scenes look at how to create your own niche and surround yourself with people who have the same standards for themselves and the same sense of quality.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/5ikc5ciw8zgtl091/s_eef10010_podcast_play_79859057_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432266-44100-2-308d03888bc1c1ec.mp3" length="93952042" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Alice Valder Curran sits down with us to talk about her impressive career, why she ultimately chose Hogan Lovells as her employer, and what it takes to be successful in this area of the industry, even in times when you can only work part-time. Alice gives us a behind-the-scenes look at how to create your own niche and surround yourself with people who have the same standards for themselves and the same sense of quality.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2348</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>5</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking the Cure - Exploring the industry with Randy Prebula</title>
        <itunes:title>Talking the Cure - Exploring the industry with Randy Prebula</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-randy-prebula/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-randy-prebula/#comments</comments>        <pubDate>Tue, 24 Oct 2023 00:30:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/d664c775-9473-3b60-b510-e5698daa70af</guid>
                                    <description><![CDATA[In this episode, Randy Prebular sits down with us and we talk about his impressive professional career, how he actually wanted to be a pediatrician at the beginning of his career, and how he then went from being a research scientist to a partner in a major law firm. We hear many exciting anecdotes, Randy gives us a behind-the-scenes look and tips on how young lawyers can make their careers more successful.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Randy Prebular sits down with us and we talk about his impressive professional career, how he actually wanted to be a pediatrician at the beginning of his career, and how he then went from being a research scientist to a partner in a major law firm. We hear many exciting anecdotes, Randy gives us a behind-the-scenes look and tips on how young lawyers can make their careers more successful.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/z16i6ovzocmn4xqo/s_eef10010_podcast_play_79859092_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432301-44100-2-a6b7b92e5e0131bc.mp3" length="111523089" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Randy Prebular sits down with us and we talk about his impressive professional career, how he actually wanted to be a pediatrician at the beginning of his career, and how he then went from being a research scientist to a partner in a major law firm. We hear many exciting anecdotes, Randy gives us a behind-the-scenes look and tips on how young lawyers can make their careers more successful.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2788</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>4</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking the Cure - Discussing the implications of the Inflation Reduction Act (IRA)</title>
        <itunes:title>Talking the Cure - Discussing the implications of the Inflation Reduction Act (IRA)</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-implications-of-the-inflation-reduction-act-ira/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-implications-of-the-inflation-reduction-act-ira/#comments</comments>        <pubDate>Thu, 28 Sep 2023 11:19:00 +0200</pubDate>
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                                    <description><![CDATA[In this podcast episode, Alice Curran and Cullen Taylor discuss the implications of the Inflation Reduction Act (IRA) on the life sciences and healthcare sector. They explore how IRA can impact drug pricing, development, collaboration, and partnerships. The episode covers assessing IRA’s impact, economic provisions in agreements, launch strategies, backup compounds, fixed-dose combinations, and the challenges of out-licensing. They highlight the complexities and potential risks in dealing with IRA.]]></description>
                                                            <content:encoded><![CDATA[In this podcast episode, Alice Curran and Cullen Taylor discuss the implications of the Inflation Reduction Act (IRA) on the life sciences and healthcare sector. They explore how IRA can impact drug pricing, development, collaboration, and partnerships. The episode covers assessing IRA’s impact, economic provisions in agreements, launch strategies, backup compounds, fixed-dose combinations, and the challenges of out-licensing. They highlight the complexities and potential risks in dealing with IRA.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/zc8jjvrzch09m8re/s_eef10010_podcast_play_79859087_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432308-48000-2-7d819f3bc0e33aae.mp3" length="75544320" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this podcast episode, Alice Curran and Cullen Taylor discuss the implications of the Inflation Reduction Act (IRA) on the life sciences and healthcare sector. They explore how IRA can impact drug pricing, development, collaboration, and partnerships. The episode covers assessing IRA’s impact, economic provisions in agreements, launch strategies, backup compounds, fixed-dose combinations, and the challenges of out-licensing. They highlight the complexities and potential risks in dealing with IRA.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1888</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>3</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Discussing latest developments​ іn clinical trials diversity, driven​ by FDORA</title>
        <itunes:title>Talking the Cure - Discussing latest developments​ іn clinical trials diversity, driven​ by FDORA</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-latest-developments%e2%80%8b-%d1%96n-clinical-trials-diversity-driven%e2%80%8b-by-fdora/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-latest-developments%e2%80%8b-%d1%96n-clinical-trials-diversity-driven%e2%80%8b-by-fdora/#comments</comments>        <pubDate>Wed, 06 Sep 2023 11:52:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/6889f14e-014d-3b8f-ac4e-4f7168e3f2f3</guid>
                                    <description><![CDATA[In this episode​ оf 'Talking the Cure,'​ we dive into the latest developments​ іn clinical trials diversity, driven​ by the Food and Drug Omnibus Reform Act (FDORA). Join Stephanie Agu, Akosua Tuffuor and Deborah Cho​ as​ we explore FDORA's key provisions related to diversity action plans.
We'll briefly summarize the history​ оf FDA's efforts​ іn this area, discuss the impact​ оf FDORA, examine the challenges and unknowns​ іt presents​ tо sponsors, including what constitutes adequate diversity, potential data collection hurdles, and highlight upcoming FDA public workshops and guidances.
If you are interested in more information all around Hogan Lovells Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></description>
                                                            <content:encoded><![CDATA[In this episode​ оf 'Talking the Cure,'​ we dive into the latest developments​ іn clinical trials diversity, driven​ by the Food and Drug Omnibus Reform Act (FDORA). Join Stephanie Agu, Akosua Tuffuor and Deborah Cho​ as​ we explore FDORA's key provisions related to diversity action plans.
We'll briefly summarize the history​ оf FDA's efforts​ іn this area, discuss the impact​ оf FDORA, examine the challenges and unknowns​ іt presents​ tо sponsors, including what constitutes adequate diversity, potential data collection hurdles, and highlight upcoming FDA public workshops and guidances.
If you are interested in more information all around Hogan Lovells Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/2xypvx7fp4c9tthx/s_eef10010_podcast_play_79859067_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432312-44100-2-f1fa0cba151f58c2.mp3" length="47958725" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode​ оf 'Talking the Cure,'​ we dive into the latest developments​ іn clinical trials diversity, driven​ by the Food and Drug Omnibus Reform Act (FDORA). Join Stephanie Agu, Akosua Tuffuor and Deborah Cho​ as​ we explore FDORA's key provisions related to diversity action plans.
We'll briefly summarize the history​ оf FDA's efforts​ іn this area, discuss the impact​ оf FDORA, examine the challenges and unknowns​ іt presents​ tо sponsors, including what constitutes adequate diversity, potential data collection hurdles, and highlight upcoming FDA public workshops and guidances.
If you are interested in more information all around Hogan Lovells Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1198</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>2</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Discussing Artificial Intelligence in Medical Devices</title>
        <itunes:title>Talking the Cure - Discussing Artificial Intelligence in Medical Devices</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-artificial-intelligence-in-medical-devices/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-artificial-intelligence-in-medical-devices/#comments</comments>        <pubDate>Thu, 26 Jan 2023 06:00:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/0f5af3c1-4ad1-3b0e-8195-0db6b06156be</guid>
                                    <description><![CDATA[Arne Thiermann and Nicole Saurin talk about the current state and development of artificial intelligence in the medical device industry. How will AI medical devices be classified by the AIA Proposal? What is the relationship between the AIA Proposal and the MDR? What laws apply to the liability of medical AI products? Who is liable if the AI application makes a wrong decision? And a lot more questions about the regulations and potential liability issues around AI in the MedTech industry.]]></description>
                                                            <content:encoded><![CDATA[Arne Thiermann and Nicole Saurin talk about the current state and development of artificial intelligence in the medical device industry. How will AI medical devices be classified by the AIA Proposal? What is the relationship between the AIA Proposal and the MDR? What laws apply to the liability of medical AI products? Who is liable if the AI application makes a wrong decision? And a lot more questions about the regulations and potential liability issues around AI in the MedTech industry.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/9056z2l13a4zrlkl/s_eef10010_podcast_play_79859088_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432307-48000-2-378ad4a77b98302f.mp3" length="83418310" type="audio/mpeg"/>
                <itunes:summary><![CDATA[Arne Thiermann and Nicole Saurin talk about the current state and development of artificial intelligence in the medical device industry. How will AI medical devices be classified by the AIA Proposal? What is the relationship between the AIA Proposal and the MDR? What laws apply to the liability of medical AI products? Who is liable if the AI application makes a wrong decision? And a lot more questions about the regulations and potential liability issues around AI in the MedTech industry.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2085</itunes:duration>
        <itunes:season>4</itunes:season>
        <itunes:episode>1</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Discussing MedTech Color with Kwame Ulmer</title>
        <itunes:title>Talking the Cure - Discussing MedTech Color with Kwame Ulmer</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-medtech-color-with-kwame-ulmer/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-medtech-color-with-kwame-ulmer/#comments</comments>        <pubDate>Mon, 14 Nov 2022 00:00:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/7d22d83c-f7e2-3595-a7c4-98b3467e8d61</guid>
                                    <description><![CDATA[In this episode, Beth L. Roberts (Partner, Washington, D.C.) is talking to Kwame Ulmer (Founder and Executive Director) about MedTech Color, its mission, programs, and resources they provide. In addition, they’re discussing which hot topics in diversity and inclusion should medical devices, pharma, and other healthcare companies should be aware of, best practices regarding diversity recruitment and retention efforts as well as how to get involved with MedTech Color and take action in their day-to-day business to help advance the representation of persons of color in the medical device industry.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Beth L. Roberts (Partner, Washington, D.C.) is talking to Kwame Ulmer (Founder and Executive Director) about MedTech Color, its mission, programs, and resources they provide. In addition, they’re discussing which hot topics in diversity and inclusion should medical devices, pharma, and other healthcare companies should be aware of, best practices regarding diversity recruitment and retention efforts as well as how to get involved with MedTech Color and take action in their day-to-day business to help advance the representation of persons of color in the medical device industry.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/g4s5lyg9zztpbxsu/s_eef10010_podcast_play_79859074_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432309-48000-2-aed2086d826c5f11.mp3" length="51152710" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Beth L. Roberts (Partner, Washington, D.C.) is talking to Kwame Ulmer (Founder and Executive Director) about MedTech Color, its mission, programs, and resources they provide. In addition, they’re discussing which hot topics in diversity and inclusion should medical devices, pharma, and other healthcare companies should be aware of, best practices regarding diversity recruitment and retention efforts as well as how to get involved with MedTech Color and take action in their day-to-day business to help advance the representation of persons of color in the medical device industry.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1278</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>7</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Exploring the industry with Ina Brock</title>
        <itunes:title>Talking the Cure - Exploring the industry with Ina Brock</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-ina-brock/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-ina-brock/#comments</comments>        <pubDate>Wed, 28 Sep 2022 00:00:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/1d01dd1e-ab5c-357b-86e4-d078b173a721</guid>
                                    <description><![CDATA[In this episode, Ina Brock invites us to her home and tells us that she actually wanted to become a journalist, but chance brought her to law. And the result of this decision is an impressive career, which we review together, Ina gives us insights into her daily work and how she sees the future of the Life Sciences &amp; Healthcare Industry.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Ina Brock invites us to her home and tells us that she actually wanted to become a journalist, but chance brought her to law. And the result of this decision is an impressive career, which we review together, Ina gives us insights into her daily work and how she sees the future of the Life Sciences &amp; Healthcare Industry.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/fbp8dx2q1dc592hs/s_eef10010_podcast_play_79859097_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432319-48000-2-5edb4b2ebde36654.mp3" length="116983750" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Ina Brock invites us to her home and tells us that she actually wanted to become a journalist, but chance brought her to law. And the result of this decision is an impressive career, which we review together, Ina gives us insights into her daily work and how she sees the future of the Life Sciences &amp; Healthcare Industry.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2924</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>6</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Discussing diversity in clinical trials</title>
        <itunes:title>Talking the Cure - Discussing diversity in clinical trials</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-diversity-in-clinical-trials/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-diversity-in-clinical-trials/#comments</comments>        <pubDate>Thu, 28 Jul 2022 09:13:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/e0c032f0-1c8c-3da6-baa4-dcbec0f61586</guid>
                                    <description><![CDATA[Robert F. Church, Sarah Thompson Schick, Stephanie Agu, and Akosua Tuffuor, J.D. discuss recent developments in FDA’s and industry’s approaches towards clinical trials and ensuring meaningful trial participation from members of historically underrepresented populations.]]></description>
                                                            <content:encoded><![CDATA[Robert F. Church, Sarah Thompson Schick, Stephanie Agu, and Akosua Tuffuor, J.D. discuss recent developments in FDA’s and industry’s approaches towards clinical trials and ensuring meaningful trial participation from members of historically underrepresented populations.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/36g0tyiqz038ane2/s_eef10010_podcast_play_79859066_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432277-48000-2-0a8642bbd2b57579.mp3" length="86489323" type="audio/mpeg"/>
                <itunes:summary><![CDATA[Robert F. Church, Sarah Thompson Schick, Stephanie Agu, and Akosua Tuffuor, J.D. discuss recent developments in FDA’s and industry’s approaches towards clinical trials and ensuring meaningful trial participation from members of historically underrepresented populations.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2162</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>6</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Discussing the repurpose of existing UK offices/retail to laboratory space?</title>
        <itunes:title>Talking the Cure - Discussing the repurpose of existing UK offices/retail to laboratory space?</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-repurpose-of-existing-uk-officesretail-to-laboratory-space/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-repurpose-of-existing-uk-officesretail-to-laboratory-space/#comments</comments>        <pubDate>Mon, 20 Jun 2022 10:33:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/9b6b52a3-575a-3060-8627-85a7d7a7528d</guid>
                                    <description><![CDATA[What to expect if you want to repurpose existing UK real estate, in particular, offices/retail to laboratory space? Graham Cutts will give an overview of potential building reconfigurations, occupier profiles, and the current industry hot topic for building owners: who bears the risk of a power outage and potential data breach?]]></description>
                                                            <content:encoded><![CDATA[What to expect if you want to repurpose existing UK real estate, in particular, offices/retail to laboratory space? Graham Cutts will give an overview of potential building reconfigurations, occupier profiles, and the current industry hot topic for building owners: who bears the risk of a power outage and potential data breach?]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/fd9uuu4ehzaaeus0/s_eef10010_podcast_play_79859082_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432296-48000-2-99c8f320db26d6d3.mp3" length="77180160" type="audio/mpeg"/>
                <itunes:summary><![CDATA[What to expect if you want to repurpose existing UK real estate, in particular, offices/retail to laboratory space? Graham Cutts will give an overview of potential building reconfigurations, occupier profiles, and the current industry hot topic for building owners: who bears the risk of a power outage and potential data breach?]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1929</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>5</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Discussing what’s on the horizons for orthopedic devices</title>
        <itunes:title>Talking the Cure - Discussing what’s on the horizons for orthopedic devices</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-what-s-on-the-horizons-for-orthopedic-devices/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-what-s-on-the-horizons-for-orthopedic-devices/#comments</comments>        <pubDate>Thu, 19 May 2022 00:01:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/b261c5c5-2469-350a-80f4-83fe542fe825</guid>
                                    <description><![CDATA[What’s on the horizons for orthopedic devices? In this episode, Michael Kasser and Jemin Jay Dedania talk about their journey in the field of orthopedic devices, why orthopedics is still a little like the wild west of the FDA, how new technologies will reshape the conduct of clinical trials, and the do’s and don’ts, when working with the FDA.]]></description>
                                                            <content:encoded><![CDATA[What’s on the horizons for orthopedic devices? In this episode, Michael Kasser and Jemin Jay Dedania talk about their journey in the field of orthopedic devices, why orthopedics is still a little like the wild west of the FDA, how new technologies will reshape the conduct of clinical trials, and the do’s and don’ts, when working with the FDA.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/in9plehgsyy55kei/s_eef10010_podcast_play_79859065_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432281-48000-2-a7a818412253c3d3.mp3" length="75450240" type="audio/mpeg"/>
                <itunes:summary><![CDATA[What’s on the horizons for orthopedic devices? In this episode, Michael Kasser and Jemin Jay Dedania talk about their journey in the field of orthopedic devices, why orthopedics is still a little like the wild west of the FDA, how new technologies will reshape the conduct of clinical trials, and the do’s and don’ts, when working with the FDA.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1886</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>4</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Exploring the industry with Andreas von Falck</title>
        <itunes:title>Talking the Cure - Exploring the industry with Andreas von Falck</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-andreas-von-falck/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-andreas-von-falck/#comments</comments>        <pubDate>Thu, 14 Apr 2022 00:00:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/fed2e2d8-d6b2-3f2f-9fd7-7c60054b270e</guid>
                                    <description><![CDATA[In this episode, Andreas von Falck will tell us that he actually wanted to work for an NGO, but then followed his father’s path and became one of the most successful patent attorneys in Germany. Andreas will tell us how he came to his Life Sciences mandates, which case influenced him the most, and what he considers to be the three most important points that the next generation should consider in order to leave their footprint in a large law firm.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Andreas von Falck will tell us that he actually wanted to work for an NGO, but then followed his father’s path and became one of the most successful patent attorneys in Germany. Andreas will tell us how he came to his Life Sciences mandates, which case influenced him the most, and what he considers to be the three most important points that the next generation should consider in order to leave their footprint in a large law firm.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/8lu7f105te9rmz2r/s_eef10010_podcast_play_79859053_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432265-48000-2-01e5c32f782e736e.mp3" length="82984363" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Andreas von Falck will tell us that he actually wanted to work for an NGO, but then followed his father’s path and became one of the most successful patent attorneys in Germany. Andreas will tell us how he came to his Life Sciences mandates, which case influenced him the most, and what he considers to be the three most important points that the next generation should consider in order to leave their footprint in a large law firm.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2074</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>3</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure: Discussing Digital Health Applications in Germany</title>
        <itunes:title>Talking the Cure: Discussing Digital Health Applications in Germany</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-digital-health-applications-in-germany/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-digital-health-applications-in-germany/#comments</comments>        <pubDate>Wed, 23 Mar 2022 23:01:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/7ac35e93-1de6-3cd6-a689-b8ea3cb433ba</guid>
                                    <description><![CDATA[In this episode, Dr. Victor Stephani, Chief Of Staff at the German digital health high flyer HelloBetter, and Arne Thiermann, a life sciences partner in the Hamburg office and very familiar with the regulations of digital health applications, discuss the exciting yet rocky road bringing a digital health application into reimbursement by German social security. Victor took us behind the scenes to share how HelloBetter had six successful fast track processes at BfArM and his tips for anyone planning to follow.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Dr. Victor Stephani, Chief Of Staff at the German digital health high flyer HelloBetter, and Arne Thiermann, a life sciences partner in the Hamburg office and very familiar with the regulations of digital health applications, discuss the exciting yet rocky road bringing a digital health application into reimbursement by German social security. Victor took us behind the scenes to share how HelloBetter had six successful fast track processes at BfArM and his tips for anyone planning to follow.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/4qpe2neinay6jg4l/s_eef10010_podcast_play_79859086_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432299-48000-2-493d1fee247834c5.mp3" length="83389440" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Dr. Victor Stephani, Chief Of Staff at the German digital health high flyer HelloBetter, and Arne Thiermann, a life sciences partner in the Hamburg office and very familiar with the regulations of digital health applications, discuss the exciting yet rocky road bringing a digital health application into reimbursement by German social security. Victor took us behind the scenes to share how HelloBetter had six successful fast track processes at BfArM and his tips for anyone planning to follow.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2084</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>2</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure - Exploring the industry with Jonathan S. Kahan</title>
        <itunes:title>Talking the Cure - Exploring the industry with Jonathan S. Kahan</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jonathan-s-kahan/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jonathan-s-kahan/#comments</comments>        <pubDate>Wed, 02 Mar 2022 11:30:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/1ecb1fba-ef44-384d-9d28-e76dd8281405</guid>
                                    <description><![CDATA[In the first episodes of Season 3, Jonathan S. Kahan, partner and passionate lawyer in the Medical Device and Technology Regulatory practice, took the time to talk to our host, Julius Bülow, about his work as a lawyer, how he built his practice from the ground up and what talents he discovered along the way, what continues to excite him about his work, and we find out that he was already portraying the digitization of health care two decades ago.]]></description>
                                                            <content:encoded><![CDATA[In the first episodes of Season 3, Jonathan S. Kahan, partner and passionate lawyer in the Medical Device and Technology Regulatory practice, took the time to talk to our host, Julius Bülow, about his work as a lawyer, how he built his practice from the ground up and what talents he discovered along the way, what continues to excite him about his work, and we find out that he was already portraying the digitization of health care two decades ago.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/zhs7gcwpc6zw6lgd/s_eef10010_podcast_play_79859091_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432317-44100-2-3ca082621730f865.mp3" length="85703691" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In the first episodes of Season 3, Jonathan S. Kahan, partner and passionate lawyer in the Medical Device and Technology Regulatory practice, took the time to talk to our host, Julius Bülow, about his work as a lawyer, how he built his practice from the ground up and what talents he discovered along the way, what continues to excite him about his work, and we find out that he was already portraying the digitization of health care two decades ago.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2677</itunes:duration>
        <itunes:season>3</itunes:season>
        <itunes:episode>1</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure: Discussing Early Access Programs (EAPs) in the US and Germany</title>
        <itunes:title>Talking the Cure: Discussing Early Access Programs (EAPs) in the US and Germany</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-early-access-programs-eaps-in-the-us-and-germany/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-early-access-programs-eaps-in-the-us-and-germany/#comments</comments>        <pubDate>Thu, 16 Dec 2021 11:34:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/696a7693-f3d5-3389-875b-e0bf22707723</guid>
                                    <description><![CDATA[In this episode, I talk with Dr. Tina Welter-Birk and Komal Karnik Nigam about the Early Access Programs (EAPs), known as Expanded Access Programs in the US, in Germany, and the United States, which allow pre-approval access to medicines for certain patients. While the name of EAPs varies by country, there are two main types of early access programs in Europe; Compassionate Use Programs (CUPs) and Named-Patient Programs (NPPs). Both of these differ in certain ways to typical Expanded Access Programs in the US and with this podcast, we‘re trying to shed some light on whats to consider entering these programs. Overall an interesting overview of the Early Access Programs (EAPs), which you should listen to if you‘re interested in this field.]]></description>
                                                            <content:encoded><![CDATA[In this episode, I talk with Dr. Tina Welter-Birk and Komal Karnik Nigam about the Early Access Programs (EAPs), known as Expanded Access Programs in the US, in Germany, and the United States, which allow pre-approval access to medicines for certain patients. While the name of EAPs varies by country, there are two main types of early access programs in Europe; Compassionate Use Programs (CUPs) and Named-Patient Programs (NPPs). Both of these differ in certain ways to typical Expanded Access Programs in the US and with this podcast, we‘re trying to shed some light on whats to consider entering these programs. Overall an interesting overview of the Early Access Programs (EAPs), which you should listen to if you‘re interested in this field.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/wbh3ezd93nd6ej2e/s_eef10010_podcast_play_79859073_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432295-44100-2-795a8c41b5370a68.mp3" length="64263851" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, I talk with Dr. Tina Welter-Birk and Komal Karnik Nigam about the Early Access Programs (EAPs), known as Expanded Access Programs in the US, in Germany, and the United States, which allow pre-approval access to medicines for certain patients. While the name of EAPs varies by country, there are two main types of early access programs in Europe; Compassionate Use Programs (CUPs) and Named-Patient Programs (NPPs). Both of these differ in certain ways to typical Expanded Access Programs in the US and with this podcast, we‘re trying to shed some light on whats to consider entering these programs. Overall an interesting overview of the Early Access Programs (EAPs), which you should listen to if you‘re interested in this field.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1998</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>9</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Exploring the industry with Christian Di Mauro</title>
        <itunes:title>Talking The Cure: Exploring the industry with Christian Di Mauro</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-christian-di-mauro/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-christian-di-mauro/#comments</comments>        <pubDate>Wed, 01 Dec 2021 11:02:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/7bd2677e-d088-36e3-beae-03dec94e5db8</guid>
                                    <description><![CDATA[In this episode, Christian Di Mauro, who is heading the Italian litigation and arbitration practice talk about his 17 years of experience working with the Life Sciences and Health Care industry and being involved in products including pharmaceuticals, vaccines, medical devices. He is also discussing the interesting role he is in, including his ability to advise Italian and French law as a litigator, his biggest matter, how he approaches his job, and what he does for his work-life balance.
You can find additional thought leadership and information regarding digital health on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Christian Di Mauro, who is heading the Italian litigation and arbitration practice talk about his 17 years of experience working with the Life Sciences and Health Care industry and being involved in products including pharmaceuticals, vaccines, medical devices. He is also discussing the interesting role he is in, including his ability to advise Italian and French law as a litigator, his biggest matter, how he approaches his job, and what he does for his work-life balance.
You can find additional thought leadership and information regarding digital health on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/txvokelcap3t00cp/s_eef10010_podcast_play_79859064_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432292-44100-2-4e21329b0f8052fc.mp3" length="58080551" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Christian Di Mauro, who is heading the Italian litigation and arbitration practice talk about his 17 years of experience working with the Life Sciences and Health Care industry and being involved in products including pharmaceuticals, vaccines, medical devices. He is also discussing the interesting role he is in, including his ability to advise Italian and French law as a litigator, his biggest matter, how he approaches his job, and what he does for his work-life balance.
You can find additional thought leadership and information regarding digital health on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1810</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>9</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing return to work policies, testing at work sites, and vaccinations</title>
        <itunes:title>Talking The Cure: Discussing return to work policies, testing at work sites, and vaccinations</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-return-to-work-policies-testing-at-work-sites-and-vaccinations/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-return-to-work-policies-testing-at-work-sites-and-vaccinations/#comments</comments>        <pubDate>Tue, 06 Jul 2021 12:32:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/9510df1e-d929-3883-a98d-e44978a7e18e</guid>
                                    <description><![CDATA[In this episode, Thierry Meillat, Stefan Martin, Eckard Schwarz, and Zachary Siegel talked about the various return to work policies, testing at work sites, mask mandates, and vaccinations. Due to the fast developments of the situation, a few comments are already outdated, but this didn't take away any of the essences of the conversation.
You can find additional thought leadership and information regarding digital health on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Thierry Meillat, Stefan Martin, Eckard Schwarz, and Zachary Siegel talked about the various return to work policies, testing at work sites, mask mandates, and vaccinations. Due to the fast developments of the situation, a few comments are already outdated, but this didn't take away any of the essences of the conversation.
You can find additional thought leadership and information regarding digital health on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/w4n8rqjixqq8m3ea/s_eef10010_podcast_play_79859071_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432298-44100-2-3c8a4f6644339e83.mp3" length="64287568" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Thierry Meillat, Stefan Martin, Eckard Schwarz, and Zachary Siegel talked about the various return to work policies, testing at work sites, mask mandates, and vaccinations. Due to the fast developments of the situation, a few comments are already outdated, but this didn't take away any of the essences of the conversation.
You can find additional thought leadership and information regarding digital health on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1994</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>8</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Exploring the industry with Lowell Zeta</title>
        <itunes:title>Talking The Cure: Exploring the industry with Lowell Zeta</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-lowell-zeta/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-lowell-zeta/#comments</comments>        <pubDate>Tue, 15 Jun 2021 14:06:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/82bd21c1-c180-3bd9-b23e-e7b1929e4de3</guid>
                                    <description><![CDATA[In this episode, Lowell M. Zeta, who just rejoined the firm after serving as Senior Counselor to the Commissioner at FDA, is going to talk to Philip Katz about his work on cross-cutting and high-priority initiatives promoting innovation and addressing public health issues, including the COVID-19 pandemic response and the decision to make the move back to Hogan Lovells.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Lowell M. Zeta, who just rejoined the firm after serving as Senior Counselor to the Commissioner at FDA, is going to talk to Philip Katz about his work on cross-cutting and high-priority initiatives promoting innovation and addressing public health issues, including the COVID-19 pandemic response and the decision to make the move back to Hogan Lovells.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/9mwezp0jb5hz8aqy/s_eef10010_podcast_play_79859075_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432303-44100-2-fddf9a2c30727854.mp3" length="59955085" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Lowell M. Zeta, who just rejoined the firm after serving as Senior Counselor to the Commissioner at FDA, is going to talk to Philip Katz about his work on cross-cutting and high-priority initiatives promoting innovation and addressing public health issues, including the COVID-19 pandemic response and the decision to make the move back to Hogan Lovells.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1859</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>7</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing the impact of Covid-19 on cell, tissue, and gene therapy products</title>
        <itunes:title>Talking The Cure: Discussing the impact of Covid-19 on cell, tissue, and gene therapy products</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-impact-of-covid-19-on-cell-tissue-and-gene-therapy-products/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-impact-of-covid-19-on-cell-tissue-and-gene-therapy-products/#comments</comments>        <pubDate>Thu, 06 May 2021 14:30:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/6389c581-3123-3d87-93c6-152114aa491e</guid>
                                    <description><![CDATA[In this episode, I talk with Michael Druckman, Jane Kalinina and Bert Lao about the the impact of Covid-19 on cell, tissue, and gene therapy products. We touch base on the enforcement discretion for tissue products and those transitioning under explicit enforcement and approval to satisfy good manufacturing practices under the FDA. In addition, we focus on orphan drug sameness and individualized therapies issues. Overall an interesting overview on the cell, tissue, and gene therapy products and its market developments.]]></description>
                                                            <content:encoded><![CDATA[In this episode, I talk with Michael Druckman, Jane Kalinina and Bert Lao about the the impact of Covid-19 on cell, tissue, and gene therapy products. We touch base on the enforcement discretion for tissue products and those transitioning under explicit enforcement and approval to satisfy good manufacturing practices under the FDA. In addition, we focus on orphan drug sameness and individualized therapies issues. Overall an interesting overview on the cell, tissue, and gene therapy products and its market developments.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/w0yqcqnr5qct832x/s_eef10010_podcast_play_79859090_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432297-44100-2-eb714561afe64a0e.mp3" length="103436592" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, I talk with Michael Druckman, Jane Kalinina and Bert Lao about the the impact of Covid-19 on cell, tissue, and gene therapy products. We touch base on the enforcement discretion for tissue products and those transitioning under explicit enforcement and approval to satisfy good manufacturing practices under the FDA. In addition, we focus on orphan drug sameness and individualized therapies issues. Overall an interesting overview on the cell, tissue, and gene therapy products and its market developments.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>3210</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>6</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing advertising and promotion of COVID-19 test kits</title>
        <itunes:title>Talking The Cure: Discussing advertising and promotion of COVID-19 test kits</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-advertising-and-promotion-of-covid-19-test-kits/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-advertising-and-promotion-of-covid-19-test-kits/#comments</comments>        <pubDate>Thu, 15 Apr 2021 14:22:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/fe02874c-7370-3b32-86fd-df8973411833</guid>
                                    <description><![CDATA[In this episode, I talk with Suzanne Levy Friedman and Michael Penners about how both U.S. and Germany have seen a lot of legal/regulatory activity around advertising and promotion of COVID-19 test kits. Suzanne and Michael are giving an overview of efforts/authority with respect to regulating advertising and promotion of medical devices/products in the two jurisdictions, especially one area where this comes up frequently with clients is the increasing trend of promoting devices on social media. It was interesting to hear about these two jurisdictions and how both markets are regulated.]]></description>
                                                            <content:encoded><![CDATA[In this episode, I talk with Suzanne Levy Friedman and Michael Penners about how both U.S. and Germany have seen a lot of legal/regulatory activity around advertising and promotion of COVID-19 test kits. Suzanne and Michael are giving an overview of efforts/authority with respect to regulating advertising and promotion of medical devices/products in the two jurisdictions, especially one area where this comes up frequently with clients is the increasing trend of promoting devices on social media. It was interesting to hear about these two jurisdictions and how both markets are regulated.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/mvyj38o7conr2m0c/s_eef10010_podcast_play_79859051_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432263-44100-2-84fdb861c7277535.mp3" length="76781044" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, I talk with Suzanne Levy Friedman and Michael Penners about how both U.S. and Germany have seen a lot of legal/regulatory activity around advertising and promotion of COVID-19 test kits. Suzanne and Michael are giving an overview of efforts/authority with respect to regulating advertising and promotion of medical devices/products in the two jurisdictions, especially one area where this comes up frequently with clients is the increasing trend of promoting devices on social media. It was interesting to hear about these two jurisdictions and how both markets are regulated.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2390</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>5</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing hand sanitizers and their way to the market</title>
        <itunes:title>Talking The Cure: Discussing hand sanitizers and their way to the market</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-hand-sanitizers-and-their-way-to-the-market/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-hand-sanitizers-and-their-way-to-the-market/#comments</comments>        <pubDate>Mon, 08 Mar 2021 15:47:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/7990e34a-1ea0-3118-8913-789c3bfc9f5a</guid>
                                    <description><![CDATA[In this episode, I talk with David Horowitz about his work around bringing hand sanitizers onto the market in the US. Understanding FDA’s expectations for the guidance that opened up hand sanitizer manufacturing, including denaturants; impurities; pharmaceutical grade vs. food or industrial grade ingredients. And his pre-covid-19 regulatory over the counter drug work, overall a super interesting conversation about David's career.]]></description>
                                                            <content:encoded><![CDATA[In this episode, I talk with David Horowitz about his work around bringing hand sanitizers onto the market in the US. Understanding FDA’s expectations for the guidance that opened up hand sanitizer manufacturing, including denaturants; impurities; pharmaceutical grade vs. food or industrial grade ingredients. And his pre-covid-19 regulatory over the counter drug work, overall a super interesting conversation about David's career.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/robbksh70ktgy2v9/s_eef10010_podcast_play_79859077_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432305-44100-2-79f94f6970cb9062.mp3" length="60350631" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, I talk with David Horowitz about his work around bringing hand sanitizers onto the market in the US. Understanding FDA’s expectations for the guidance that opened up hand sanitizer manufacturing, including denaturants; impurities; pharmaceutical grade vs. food or industrial grade ingredients. And his pre-covid-19 regulatory over the counter drug work, overall a super interesting conversation about David's career.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1878</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>3</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing the current ”surge” of Digital Health Innovations in Europe</title>
        <itunes:title>Talking The Cure: Discussing the current ”surge” of Digital Health Innovations in Europe</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-current-surge-of-digital-health-innovations-in-europe/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-current-surge-of-digital-health-innovations-in-europe/#comments</comments>        <pubDate>Tue, 16 Feb 2021 11:00:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/69c8f673-0096-3a03-a146-fa7053a55e2b</guid>
                                    <description><![CDATA[In this episode, I talk with Fabien Roy and Jonas Albert about the current "surge" of Digital Health Innovations in Europe, receiving the CE-Marking, getting reimbursed for their product, and what that means for Start-Ups as well as established companies. Obviously, we touched on the ongoing Covid-19 pandemic, due to the fast developments, a few things are unfortunately already outdated, but that doesn't take away anything from this conversation and I hope you'll enjoy this as much as I did.]]></description>
                                                            <content:encoded><![CDATA[In this episode, I talk with Fabien Roy and Jonas Albert about the current "surge" of Digital Health Innovations in Europe, receiving the CE-Marking, getting reimbursed for their product, and what that means for Start-Ups as well as established companies. Obviously, we touched on the ongoing Covid-19 pandemic, due to the fast developments, a few things are unfortunately already outdated, but that doesn't take away anything from this conversation and I hope you'll enjoy this as much as I did.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/o7ll7x7d1g5ac8d4/s_eef10010_podcast_play_79859094_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432321-44100-2-a92d5b8bb4879722.mp3" length="101705373" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, I talk with Fabien Roy and Jonas Albert about the current "surge" of Digital Health Innovations in Europe, receiving the CE-Marking, getting reimbursed for their product, and what that means for Start-Ups as well as established companies. Obviously, we touched on the ongoing Covid-19 pandemic, due to the fast developments, a few things are unfortunately already outdated, but that doesn't take away anything from this conversation and I hope you'll enjoy this as much as I did.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>3167</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>2</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Exploring the industry with Jodi Scott</title>
        <itunes:title>Talking The Cure: Exploring the industry with Jodi Scott</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jodi-scott/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jodi-scott/#comments</comments>        <pubDate>Thu, 21 Jan 2021 17:14:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/64a99a49-2ef0-381d-b350-04dcebec9649</guid>
                                    <description><![CDATA[In this episode, Jodi Scott, a partner at Hogan Lovells in Denver, is going to talk about her time spent as an in-house FDA counsel with the world's largest medical device manufacturer, the state of the industry, her decision to make the move to Hogan Lovells, and her overall career.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Jodi Scott, a partner at Hogan Lovells in Denver, is going to talk about her time spent as an in-house FDA counsel with the world's largest medical device manufacturer, the state of the industry, her decision to make the move to Hogan Lovells, and her overall career.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/b41xgy2bmyd0k1ee/s_eef10010_podcast_play_79859062_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432291-44100-2-77bb4f28bee7a0ec.mp3" length="57568630" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Jodi Scott, a partner at Hogan Lovells in Denver, is going to talk about her time spent as an in-house FDA counsel with the world's largest medical device manufacturer, the state of the industry, her decision to make the move to Hogan Lovells, and her overall career.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1791</itunes:duration>
        <itunes:season>2</itunes:season>
        <itunes:episode>1</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Exploring the industry with the leads of our associate committee</title>
        <itunes:title>Talking The Cure: Exploring the industry with the leads of our associate committee</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-the-leads-of-our-associate-committee/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-the-leads-of-our-associate-committee/#comments</comments>        <pubDate>Mon, 21 Dec 2020 17:46:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/27bae0c8-d874-3400-806f-8b16a78f9e78</guid>
                                    <description><![CDATA[In this episode, I talk with Jeff Jay and Tina Welter about their involvement in the life sciences and health care associate committee. This position was created about 18 months ago to give associates more insight into the developments coming out of the leadership team. In addition, Tina and Jeff talk about their experiences with the role, their work in the life sciences and health care industry group, and how they are pursuing their career at Hogan Lovells.]]></description>
                                                            <content:encoded><![CDATA[In this episode, I talk with Jeff Jay and Tina Welter about their involvement in the life sciences and health care associate committee. This position was created about 18 months ago to give associates more insight into the developments coming out of the leadership team. In addition, Tina and Jeff talk about their experiences with the role, their work in the life sciences and health care industry group, and how they are pursuing their career at Hogan Lovells.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/ap8fjofvmxlpi63v/s_eef10010_podcast_play_79859089_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432320-44100-2-69a667bd255cd671.mp3" length="78049122" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, I talk with Jeff Jay and Tina Welter about their involvement in the life sciences and health care associate committee. This position was created about 18 months ago to give associates more insight into the developments coming out of the leadership team. In addition, Tina and Jeff talk about their experiences with the role, their work in the life sciences and health care industry group, and how they are pursuing their career at Hogan Lovells.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2435</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>20</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing artificial intelligence in drug discovery and the possible legal issues that result from this usage.</title>
        <itunes:title>Talking The Cure: Discussing artificial intelligence in drug discovery and the possible legal issues that result from this usage.</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-artificial-intelligence-in-drug-discovery-and-the-possible-legal-issues-that-result-from-this-usage/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-artificial-intelligence-in-drug-discovery-and-the-possible-legal-issues-that-result-from-this-usage/#comments</comments>        <pubDate>Thu, 03 Dec 2020 09:50:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/2951211e-bcb0-308f-81ce-564c38b7c996</guid>
                                    <description><![CDATA[In this episode, Jason Lohr and Imogen Ireland, are going to explore some interesting questions to do with whether or not patent law is set up to deal with innovations developed by AI. In the second half of the podcast, we’ll do a practical assessment of the potential legal issues stemming from the way in which AI is being used today]]></description>
                                                            <content:encoded><![CDATA[In this episode, Jason Lohr and Imogen Ireland, are going to explore some interesting questions to do with whether or not patent law is set up to deal with innovations developed by AI. In the second half of the podcast, we’ll do a practical assessment of the potential legal issues stemming from the way in which AI is being used today]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/d8gqche6thpzcxtz/s_eef10010_podcast_play_79859078_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432311-44100-2-c208db514d68722b.mp3" length="55219502" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Jason Lohr and Imogen Ireland, are going to explore some interesting questions to do with whether or not patent law is set up to deal with innovations developed by AI. In the second half of the podcast, we’ll do a practical assessment of the potential legal issues stemming from the way in which AI is being used today]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2296</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>19</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing in vitro diagnostics (IVD) in times of a pandemic</title>
        <itunes:title>Talking The Cure: Discussing in vitro diagnostics (IVD) in times of a pandemic</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-in-vitro-diagnostics-ivd-in-times-of-a-pandemic/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-in-vitro-diagnostics-ivd-in-times-of-a-pandemic/#comments</comments>        <pubDate>Fri, 13 Nov 2020 10:56:00 +0100</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/92f51c58-02c9-3b23-bdb0-41957da726cf</guid>
                                    <description><![CDATA[In this episode, Randy J. Prebula, Susan D. Tiedy-Stevenson, and Erkang Ai, Ph.D. are talking about the “world” of what is considered to be in in-vitro diagnostics, the current SARS-CoV-2 situation, and the various IVD’s that are being granted Emergency Use Authorization by the FDA.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Randy J. Prebula, Susan D. Tiedy-Stevenson, and Erkang Ai, Ph.D. are talking about the “world” of what is considered to be in in-vitro diagnostics, the current SARS-CoV-2 situation, and the various IVD’s that are being granted Emergency Use Authorization by the FDA.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/t7upe8bifexi4kjk/s_eef10010_podcast_play_79859054_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432285-44100-2-8907ad7ff869b95b.mp3" length="35460121" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Randy J. Prebula, Susan D. Tiedy-Stevenson, and Erkang Ai, Ph.D. are talking about the “world” of what is considered to be in in-vitro diagnostics, the current SARS-CoV-2 situation, and the various IVD’s that are being granted Emergency Use Authorization by the FDA.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2083</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>18</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking The Cure: Exploring the industry with Jonathan Wasserman</title>
        <itunes:title>Talking The Cure: Exploring the industry with Jonathan Wasserman</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jonathan-wasserman/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jonathan-wasserman/#comments</comments>        <pubDate>Wed, 21 Oct 2020 17:03:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/e2c63078-5855-3036-bb85-d1263ea2e25d</guid>
                                    <description><![CDATA[Jon Wasserman, a new partner at Hogan Lovells and former Bristol Myers Squibb vice president, is going to talk about his past, the state of the industry, his decision to make the move to Hogan Lovells, and a potential dinner with two British gentlemen and Abraham Lincoln.]]></description>
                                                            <content:encoded><![CDATA[Jon Wasserman, a new partner at Hogan Lovells and former Bristol Myers Squibb vice president, is going to talk about his past, the state of the industry, his decision to make the move to Hogan Lovells, and a potential dinner with two British gentlemen and Abraham Lincoln.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/n3me5mzatas82vmo/s_eef10010_podcast_play_79859056_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432300-44100-1-cb170bef2ae5fe1e.mp3" length="27664042" type="audio/mpeg"/>
                <itunes:summary><![CDATA[Jon Wasserman, a new partner at Hogan Lovells and former Bristol Myers Squibb vice president, is going to talk about his past, the state of the industry, his decision to make the move to Hogan Lovells, and a potential dinner with two British gentlemen and Abraham Lincoln.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2246</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>17</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking The Cure: Discussing the “Buy America” Executive Order</title>
        <itunes:title>Talking The Cure: Discussing the “Buy America” Executive Order</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-buy-america-executive-order/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-buy-america-executive-order/#comments</comments>        <pubDate>Mon, 12 Oct 2020 17:33:00 +0200</pubDate>
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                                    <description><![CDATA[On August 6, 2020, U.S. President Donald Trump issued his much-anticipated "Buy American" Executive Order (EO), aimed at shoring up domestic manufacture of "essential medicines", "medical countermeasures", and "critical inputs" (API and other raw materials), and decreasing dependency on non-domestic sources.

Philip Katz leads a discussion with Joy Sturm, Mike Heyl, Kelly Ann Shaw, and David Horowitz about what they're seeing, what they expect, and what actions companies are – or should be – taking or considering.]]></description>
                                                            <content:encoded><![CDATA[On August 6, 2020, U.S. President Donald Trump issued his much-anticipated "Buy American" Executive Order (EO), aimed at shoring up domestic manufacture of "essential medicines", "medical countermeasures", and "critical inputs" (API and other raw materials), and decreasing dependency on non-domestic sources.

Philip Katz leads a discussion with Joy Sturm, Mike Heyl, Kelly Ann Shaw, and David Horowitz about what they're seeing, what they expect, and what actions companies are – or should be – taking or considering.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/tgacvtdba013pxg2/s_eef10010_podcast_play_79859098_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432324-44100-2-67ae55558814fbb9.mp3" length="130681237" type="audio/mpeg"/>
                <itunes:summary><![CDATA[On August 6, 2020, U.S. President Donald Trump issued his much-anticipated "Buy American" Executive Order (EO), aimed at shoring up domestic manufacture of "essential medicines", "medical countermeasures", and "critical inputs" (API and other raw materials), and decreasing dependency on non-domestic sources.

Philip Katz leads a discussion with Joy Sturm, Mike Heyl, Kelly Ann Shaw, and David Horowitz about what they're seeing, what they expect, and what actions companies are – or should be – taking or considering.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>3267</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>16</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing opportunities and risks for international digital health companies engaging in Germany</title>
        <itunes:title>Talking The Cure: Discussing opportunities and risks for international digital health companies engaging in Germany</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-opportunities-and-risks-for-international-digital-health-companies-engaging-in-germany/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-opportunities-and-risks-for-international-digital-health-companies-engaging-in-germany/#comments</comments>        <pubDate>Mon, 12 Oct 2020 16:42:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/4b465007-c255-33e5-9177-f460330727df</guid>
                                    <description><![CDATA[In this episode, Arne Thiermann and Dr. Julian Braun, director of legal at Heartbeat Labs, discuss the opportunities and risks for international companies planning to enter the German market in the digital health sector, especially with regard to reimbursement and the impact of regulatory changes in Germany.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Arne Thiermann and Dr. Julian Braun, director of legal at Heartbeat Labs, discuss the opportunities and risks for international companies planning to enter the German market in the digital health sector, especially with regard to reimbursement and the impact of regulatory changes in Germany.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/5f81hpv3mg5evqlz/s_eef10010_podcast_play_79859068_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432279-44100-2-c2f3621484bdf148.mp3" length="86332646" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Arne Thiermann and Dr. Julian Braun, director of legal at Heartbeat Labs, discuss the opportunities and risks for international companies planning to enter the German market in the digital health sector, especially with regard to reimbursement and the impact of regulatory changes in Germany.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2158</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>15</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing innovation in drug development, the competitive aspects and affordability of medicines in Europe</title>
        <itunes:title>Talking The Cure: Discussing innovation in drug development, the competitive aspects and affordability of medicines in Europe</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-innovation-in-drug-development-the-competitive-aspects-and-affordability-of-medicines-in-europe/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-innovation-in-drug-development-the-competitive-aspects-and-affordability-of-medicines-in-europe/#comments</comments>        <pubDate>Mon, 12 Oct 2020 16:38:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/e94dbfbd-f938-3ad7-aecf-650581ed74fa</guid>
                                    <description><![CDATA[In this episode, May Lyn Yuen and Hein Van den Bos discuss the balance of innovation in drug development, the competitive aspects and affordability of medicines in Europe, and the changes in the regulatory environment at the EU level as well as the EU Member State level.]]></description>
                                                            <content:encoded><![CDATA[In this episode, May Lyn Yuen and Hein Van den Bos discuss the balance of innovation in drug development, the competitive aspects and affordability of medicines in Europe, and the changes in the regulatory environment at the EU level as well as the EU Member State level.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/rsdohgucmk91fg1g/s_eef10010_podcast_play_79859055_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432286-44100-2-36508e727c3ba9a4.mp3" length="35661351" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, May Lyn Yuen and Hein Van den Bos discuss the balance of innovation in drug development, the competitive aspects and affordability of medicines in Europe, and the changes in the regulatory environment at the EU level as well as the EU Member State level.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>891</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>14</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing recent industry developments with the Hogan Lovells Sciences Unit</title>
        <itunes:title>Talking The Cure: Discussing recent industry developments with the Hogan Lovells Sciences Unit</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-recent-industry-developments-with-the-hogan-lovells-sciences-unit/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-recent-industry-developments-with-the-hogan-lovells-sciences-unit/#comments</comments>        <pubDate>Mon, 12 Oct 2020 16:33:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/7b16fce0-6700-3a09-9f71-786917de4459</guid>
                                    <description><![CDATA[In our latest episode, you will get to know members of our Science Unit Dr. Marion Palmer and Dr. Rachel Gribben, who talk about their experience working in this unit for over 20 years, as well as their latest work on COVID-19 related matters. We also discuss how they are providing pro bono work and what they do to relax.]]></description>
                                                            <content:encoded><![CDATA[In our latest episode, you will get to know members of our Science Unit Dr. Marion Palmer and Dr. Rachel Gribben, who talk about their experience working in this unit for over 20 years, as well as their latest work on COVID-19 related matters. We also discuss how they are providing pro bono work and what they do to relax.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/yrthdpcsqs1qx1re/s_eef10010_podcast_play_79859093_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432314-44100-2-46f953cade2ea980.mp3" length="106919212" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In our latest episode, you will get to know members of our Science Unit Dr. Marion Palmer and Dr. Rachel Gribben, who talk about their experience working in this unit for over 20 years, as well as their latest work on COVID-19 related matters. We also discuss how they are providing pro bono work and what they do to relax.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>2672</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>13</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing the rise of telehealth in the life sciences and health care industry</title>
        <itunes:title>Talking The Cure: Discussing the rise of telehealth in the life sciences and health care industry</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-rise-of-telehealth-in-the-life-sciences-and-health-care-industry/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-rise-of-telehealth-in-the-life-sciences-and-health-care-industry/#comments</comments>        <pubDate>Mon, 12 Oct 2020 16:10:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/93aad7be-ac06-3186-a5dc-7dca5ff88950</guid>
                                    <description><![CDATA[In this episode, our partners Brooke Bumpers and William Ferreira talk about the growth of the telehealth industry during the COVID-19 pandemic and the opportunities and challenges for companies and providers in the United States and internationally. We also discuss how providers and patients are reacting to the increased use of telehealth.]]></description>
                                                            <content:encoded><![CDATA[In this episode, our partners Brooke Bumpers and William Ferreira talk about the growth of the telehealth industry during the COVID-19 pandemic and the opportunities and challenges for companies and providers in the United States and internationally. We also discuss how providers and patients are reacting to the increased use of telehealth.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/uw0wm31j1ec0qj10/s_eef10010_podcast_play_79859070_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432287-44100-2-6c200f549c110121.mp3" length="71627784" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, our partners Brooke Bumpers and William Ferreira talk about the growth of the telehealth industry during the COVID-19 pandemic and the opportunities and challenges for companies and providers in the United States and internationally. We also discuss how providers and patients are reacting to the increased use of telehealth.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1790</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>12</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Exploring the industry with Philip Katz - Part 2</title>
        <itunes:title>Talking The Cure: Exploring the industry with Philip Katz - Part 2</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-philip-katz-part-2/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-philip-katz-part-2/#comments</comments>        <pubDate>Mon, 12 Oct 2020 15:38:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/6b28709c-f74b-3b8d-9815-568eebae917a</guid>
                                    <description><![CDATA[In the second part of our two-part interview with Philip Katz, head of the Hogan Lovells Pharmaceuticals and Biotechnology Regulatory Practice, we discuss team management, diversity and we also get to learn about Phil, when he shuts down his blackberry. We had a lot to cover in our conversation with Phil, so if you haven't checked out yet, listen to the first part of our conversation.]]></description>
                                                            <content:encoded><![CDATA[In the second part of our two-part interview with Philip Katz, head of the Hogan Lovells Pharmaceuticals and Biotechnology Regulatory Practice, we discuss team management, diversity and we also get to learn about Phil, when he shuts down his blackberry. We had a lot to cover in our conversation with Phil, so if you haven't checked out yet, listen to the first part of our conversation.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/81qxca93yiqz9hmr/s_eef10010_podcast_play_79859080_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432318-44100-2-0fa9418d0b34cccd.mp3" length="54284537" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In the second part of our two-part interview with Philip Katz, head of the Hogan Lovells Pharmaceuticals and Biotechnology Regulatory Practice, we discuss team management, diversity and we also get to learn about Phil, when he shuts down his blackberry. We had a lot to cover in our conversation with Phil, so if you haven't checked out yet, listen to the first part of our conversation.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1357</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>11</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Exploring the industry with Philip Katz - Part 1</title>
        <itunes:title>Talking The Cure: Exploring the industry with Philip Katz - Part 1</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-philip-katz-part-1/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-philip-katz-part-1/#comments</comments>        <pubDate>Mon, 12 Oct 2020 15:21:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/8c9ce131-2455-31e9-bb93-e5d8eda6b102</guid>
                                    <description><![CDATA[In the first episode of our two-part interview with Philip Katz, head of the Hogan Lovells Pharmaceuticals and Biotechnology Regulatory Practice, we discuss developments in the pharmaceuticals and biotechnology industry, the global practice of law in this space, and we also get to learn about Phil and his career journey. We had a lot to cover in our conversation with Phil, so stay tuned for more industry insights in part two of our interview!]]></description>
                                                            <content:encoded><![CDATA[In the first episode of our two-part interview with Philip Katz, head of the Hogan Lovells Pharmaceuticals and Biotechnology Regulatory Practice, we discuss developments in the pharmaceuticals and biotechnology industry, the global practice of law in this space, and we also get to learn about Phil and his career journey. We had a lot to cover in our conversation with Phil, so stay tuned for more industry insights in part two of our interview!]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/xum4pzcxhwzyxdj9/s_eef10010_podcast_play_79859061_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432290-44100-2-e894af3821ac9e35.mp3" length="56420339" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In the first episode of our two-part interview with Philip Katz, head of the Hogan Lovells Pharmaceuticals and Biotechnology Regulatory Practice, we discuss developments in the pharmaceuticals and biotechnology industry, the global practice of law in this space, and we also get to learn about Phil and his career journey. We had a lot to cover in our conversation with Phil, so stay tuned for more industry insights in part two of our interview!]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1410</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>10</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure: Discussing venture capital in the life sciences and health care sector in Germany</title>
        <itunes:title>Talking the Cure: Discussing venture capital in the life sciences and health care sector in Germany</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-venture-capital-in-the-life-sciences-and-health-care-sector-in-germany/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-venture-capital-in-the-life-sciences-and-health-care-sector-in-germany/#comments</comments>        <pubDate>Mon, 12 Oct 2020 15:04:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/255ba0f0-6af9-39ec-a295-4315ba22654f</guid>
                                    <description><![CDATA[In this episode, our partners Jörg Schickert and Nikolas Zirngibl talk with Jörn Bungartz, an adviser in the digital health sector, about opportunities and barriers for venture capital in the life sciences and health care industry in Germany.
You can find additional thought leadership and information regarding venture capital in the life sciences and health care industry on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></description>
                                                            <content:encoded><![CDATA[In this episode, our partners Jörg Schickert and Nikolas Zirngibl talk with Jörn Bungartz, an adviser in the digital health sector, about opportunities and barriers for venture capital in the life sciences and health care industry in Germany.
You can find additional thought leadership and information regarding venture capital in the life sciences and health care industry on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/hitorwdblc2tcj2s/s_eef10010_podcast_play_79859081_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432313-44100-2-032944590a312427.mp3" length="61199672" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, our partners Jörg Schickert and Nikolas Zirngibl talk with Jörn Bungartz, an adviser in the digital health sector, about opportunities and barriers for venture capital in the life sciences and health care industry in Germany.
You can find additional thought leadership and information regarding venture capital in the life sciences and health care industry on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1529</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>9</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing European developments on Covid-19</title>
        <itunes:title>Talking The Cure: Discussing European developments on Covid-19</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-european-developments-on-covid-19/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-european-developments-on-covid-19/#comments</comments>        <pubDate>Mon, 12 Oct 2020 14:25:00 +0200</pubDate>
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                                    <description><![CDATA[In this episode, Elisabethann Wright, Jane Summerfield, and Hein Van den Bos talk about developments in Belgium, the UK, and the Netherlands and how the Covid-19 pandemic impacts clinical trials and the authorization process of the local authorities.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Elisabethann Wright, Jane Summerfield, and Hein Van den Bos talk about developments in Belgium, the UK, and the Netherlands and how the Covid-19 pandemic impacts clinical trials and the authorization process of the local authorities.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/6o66f66x9j3di5wl/s_eef10010_podcast_play_79859084_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432316-44100-2-0e4fc6640c8b97ac.mp3" length="62228927" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Elisabethann Wright, Jane Summerfield, and Hein Van den Bos talk about developments in Belgium, the UK, and the Netherlands and how the Covid-19 pandemic impacts clinical trials and the authorization process of the local authorities.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1555</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>8</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking The Cure: Discussing reimbursement issues in France and the MDR</title>
        <itunes:title>Talking The Cure: Discussing reimbursement issues in France and the MDR</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-reimbursement-issues-in-france-and-the-mdr/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-reimbursement-issues-in-france-and-the-mdr/#comments</comments>        <pubDate>Mon, 12 Oct 2020 14:18:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/06a51b77-f1fe-31c7-94bc-44bca9883aa1</guid>
                                    <description><![CDATA[In this episode, Charlotte Damiano and Fabien Roy talk about reimbursement issues, early access and the collection of clinical data in France. In the end they both address general developments of the medical device regulation.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Charlotte Damiano and Fabien Roy talk about reimbursement issues, early access and the collection of clinical data in France. In the end they both address general developments of the medical device regulation.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/uiyqpvbv2m7sg1il/s_eef10010_podcast_play_79859059_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432315-44100-2-d176d46a8fff6eff.mp3" length="27063901" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Charlotte Damiano and Fabien Roy talk about reimbursement issues, early access and the collection of clinical data in France. In the end they both address general developments of the medical device regulation.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>676</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>7</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking the Cure: Discussing COVID-19’s impact on FDA’s inspection program and next steps after the pandemic</title>
        <itunes:title>Talking the Cure: Discussing COVID-19’s impact on FDA’s inspection program and next steps after the pandemic</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-covid-19-s-impact-on-fda-s-inspection-program-and-next-steps-after-the-pandemic/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-covid-19-s-impact-on-fda-s-inspection-program-and-next-steps-after-the-pandemic/#comments</comments>        <pubDate>Mon, 12 Oct 2020 14:14:00 +0200</pubDate>
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                                    <description><![CDATA[In this episode, Phil Katz and Jim Johnson continue their conversation about the impact of COVID-19 on FDA’s drug inspection program and the steps companies should take now and in preparation for when the pandemic is coming to an end.
For all updates around COVID-19, visit our COVID-19 hub.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Phil Katz and Jim Johnson continue their conversation about the impact of COVID-19 on FDA’s drug inspection program and the steps companies should take now and in preparation for when the pandemic is coming to an end.
For all updates around COVID-19, visit our COVID-19 hub.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/dikisjwylt7pg3g4/s_eef10010_podcast_play_79859095_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432289-44100-2-34535ee94f468618.mp3" length="64919539" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Phil Katz and Jim Johnson continue their conversation about the impact of COVID-19 on FDA’s drug inspection program and the steps companies should take now and in preparation for when the pandemic is coming to an end.
For all updates around COVID-19, visit our COVID-19 hub.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1622</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>6</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking The Cure: Discussing how the coronavirus pandemic is affecting the pharmaceutical industry and FDA</title>
        <itunes:title>Talking The Cure: Discussing how the coronavirus pandemic is affecting the pharmaceutical industry and FDA</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-how-the-coronavirus-pandemic-is-affecting-the-pharmaceutical-industry-and-fda/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-how-the-coronavirus-pandemic-is-affecting-the-pharmaceutical-industry-and-fda/#comments</comments>        <pubDate>Mon, 12 Oct 2020 13:35:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/4c033a21-93d9-3c69-99ba-f7841784941e</guid>
                                    <description><![CDATA[In this episode, Phil Katz, David Horowitz, and Jim Johnson explore the impact on industry and FDA of the agency’s decision to halt foreign inspections and take other steps that reduce international activities. They anticipate further steps by the agency and talk about how companies can strategically address the implications, which create obstacles but also opportunities.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Phil Katz, David Horowitz, and Jim Johnson explore the impact on industry and FDA of the agency’s decision to halt foreign inspections and take other steps that reduce international activities. They anticipate further steps by the agency and talk about how companies can strategically address the implications, which create obstacles but also opportunities.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/ez4xzocif5bu5brr/s_eef10010_podcast_play_79859063_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432306-44100-2-9faa8abfcbbd58c8.mp3" length="44197136" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Phil Katz, David Horowitz, and Jim Johnson explore the impact on industry and FDA of the agency’s decision to halt foreign inspections and take other steps that reduce international activities. They anticipate further steps by the agency and talk about how companies can strategically address the implications, which create obstacles but also opportunities.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1104</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>5</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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    <item>
        <title>Talking The Cure: Discussing FDA authorities for handling a global pandemic for medical devices</title>
        <itunes:title>Talking The Cure: Discussing FDA authorities for handling a global pandemic for medical devices</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-fda-authorities-for-handling-a-global-pandemic-for-medical-devices/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-fda-authorities-for-handling-a-global-pandemic-for-medical-devices/#comments</comments>        <pubDate>Mon, 12 Oct 2020 12:53:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/b6684dd3-6921-3832-b8b0-20a07c2cc316</guid>
                                    <description><![CDATA[In this episode, Michael S. Heyl and Jonathan S. Kahan explore questions around FDA’s Emergency Use Authorization authorities, how it has been used historically, and how it may be used for the coronavirus. They highlight very recent FDA actions and project how these authorities could be applied to address supply chain issues, in addition to the development of new technologies/devices to aid in the diagnosis and treatment of the virus.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Michael S. Heyl and Jonathan S. Kahan explore questions around FDA’s Emergency Use Authorization authorities, how it has been used historically, and how it may be used for the coronavirus. They highlight very recent FDA actions and project how these authorities could be applied to address supply chain issues, in addition to the development of new technologies/devices to aid in the diagnosis and treatment of the virus.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/s4g9y3i1jrqc9u8s/s_eef10010_podcast_play_79859072_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432293-44100-2-dca99c017da47d33.mp3" length="65936238" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Michael S. Heyl and Jonathan S. Kahan explore questions around FDA’s Emergency Use Authorization authorities, how it has been used historically, and how it may be used for the coronavirus. They highlight very recent FDA actions and project how these authorities could be applied to address supply chain issues, in addition to the development of new technologies/devices to aid in the diagnosis and treatment of the virus.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1648</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>4</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking the Cure: Discussing the supply chain and its potential downfalls</title>
        <itunes:title>Talking the Cure: Discussing the supply chain and its potential downfalls</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-supply-chain-and-its-potential-downfalls/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-supply-chain-and-its-potential-downfalls/#comments</comments>        <pubDate>Mon, 12 Oct 2020 12:42:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/a114695a-7294-39e6-b697-ac46b53cc4ed</guid>
                                    <description><![CDATA[In this episode, Arne Thiermann and Mike Druckman explore questions around the supply chain in the life sciences and health care industry. They highlight the reality and the expectation when it comes down to the draft of a contract in this kind of situations.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Arne Thiermann and Mike Druckman explore questions around the supply chain in the life sciences and health care industry. They highlight the reality and the expectation when it comes down to the draft of a contract in this kind of situations.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/uixrck0g7wr2c1fs/s_eef10010_podcast_play_79859048_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432261-44100-2-af811ad4e52680e4.mp3" length="39910071" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Arne Thiermann and Mike Druckman explore questions around the supply chain in the life sciences and health care industry. They highlight the reality and the expectation when it comes down to the draft of a contract in this kind of situations.
You can find additional thought leadership and information regarding Medical Devices and Technology Regulatory on HL Engage.
If you are interested in more information all around Life Sciences and Health Care, follow us on LinkedIn and Twitter.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1633</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>3</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Exploring the industry with Jörg Schickert</title>
        <itunes:title>Talking The Cure: Exploring the industry with Jörg Schickert</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jorg-schickert/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-exploring-the-industry-with-jorg-schickert/#comments</comments>        <pubDate>Mon, 12 Oct 2020 12:39:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/edbd066b-5f4d-36b4-8492-b7e20edf3d31</guid>
                                    <description><![CDATA[In this episode, Jörg Schickert, one of the leading life sciences and health care lawyers for regulatory and commercial issues in Europe, is going to talk about his work, his views on the industry, and why he wouldn't change anything if he had the chance to start his journey all over again.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Jörg Schickert, one of the leading life sciences and health care lawyers for regulatory and commercial issues in Europe, is going to talk about his work, his views on the industry, and why he wouldn't change anything if he had the chance to start his journey all over again.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/lpr1ib5pxrgax8f7/s_eef10010_podcast_play_79859069_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432310-44100-2-bd106b31f72dcb59.mp3" length="49156295" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Jörg Schickert, one of the leading life sciences and health care lawyers for regulatory and commercial issues in Europe, is going to talk about his work, his views on the industry, and why he wouldn't change anything if he had the chance to start his journey all over again.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>1228</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>2</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
            </item>
    <item>
        <title>Talking The Cure: Discussing the use of digital tools in clinical trials</title>
        <itunes:title>Talking The Cure: Discussing the use of digital tools in clinical trials</itunes:title>
        <link>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-use-of-digital-tools-in-clinical-trials/</link>
                    <comments>https://talkingthecure.podbean.com/e/talking-the-cure-discussing-the-use-of-digital-tools-in-clinical-trials/#comments</comments>        <pubDate>Mon, 12 Oct 2020 12:22:00 +0200</pubDate>
        <guid isPermaLink="false">talkingthecurebyhoganlovells.podbean.com/e933f3b6-8dea-3d15-8e54-a572b67ffbc8</guid>
                                    <description><![CDATA[In this episode, Elisabethann Wright and Robert F. Church from our Global Regulatory practice explore questions around the use of digital tools in clinical trials and how they are regulated by international authorities. They highlight the confusion around clinical trials within the European GDPR framework.

Please rate and subscribe to our channel, so we know that you like our content.]]></description>
                                                            <content:encoded><![CDATA[In this episode, Elisabethann Wright and Robert F. Church from our Global Regulatory practice explore questions around the use of digital tools in clinical trials and how they are regulated by international authorities. They highlight the confusion around clinical trials within the European GDPR framework.

Please rate and subscribe to our channel, so we know that you like our content.]]></content:encoded>
                                    
        <enclosure url="https://mcdn.podbean.com/mf/web/tyzprlez2xm2mxti/s_eef10010_podcast_play_79859052_https_3A_2F_2Fd3ctxlq1ktw2nl_cloudfront_net_2Fstaging_2F2023-11-11_2F359432288-44100-2-73c23bf2e3a23134.mp3" length="24434221" type="audio/mpeg"/>
                <itunes:summary><![CDATA[In this episode, Elisabethann Wright and Robert F. Church from our Global Regulatory practice explore questions around the use of digital tools in clinical trials and how they are regulated by international authorities. They highlight the confusion around clinical trials within the European GDPR framework.

Please rate and subscribe to our channel, so we know that you like our content.]]></itunes:summary>
        <itunes:author>Hogan Lovells</itunes:author>
        <itunes:explicit>false</itunes:explicit>
        <itunes:block>No</itunes:block>
        <itunes:duration>961</itunes:duration>
        <itunes:season>1</itunes:season>
        <itunes:episode>1</itunes:episode>
        <itunes:episodeType>full</itunes:episodeType>
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