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<rss xmlns:itunes="http://www.itunes.com/dtds/podcast-1.0.dtd" xmlns:atom="http://www.w3.org/2005/Atom" xmlns:podcast="https://podcastindex.org/namespace/1.0" xmlns:media="http://search.yahoo.com/mrss/" version="2.0"><channel><title>Life Sciences Accelerated</title><link>https://www.spreaker.com/show/life-sciences-accelerated</link><description><![CDATA[On Life Sciences Accelerated, we discuss experiences and innovations in compliance and technology from molecule to market. <br /><br />Tune in for in-depth interviews with well-known thought leaders, and renowned subject matter experts, with unparalleled knowledge in the technology and life sciences industry.   <br /><br />We feature insightful stories that are sure to provide valuable proven new ways to connect technology, people, and data that will take your regulated business to the next level. <br /><br />Episodes will feature topics such as: Digital Transformation, IT Consulting, Pharmaceutical Compliance,  Biotech Compliance, Medical Device Compliance, and more!<br /><br />Innovative, Helpful, and thought-provoking. This is… Life Sciences Accelerated<br /><br />For more information visit, <a href="http://www.usdm.com" rel="noopener">www.usdm.com</a>.]]></description><atom:link href="https://www.spreaker.com/show/5719591/episodes/feed" rel="self" type="application/rss+xml"/><language>en</language><category>Life Sciences</category><copyright>Copyright Dan Sanchez</copyright><image><url>https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg</url><title>Life Sciences Accelerated</title><link>https://www.spreaker.com/show/life-sciences-accelerated</link></image><lastBuildDate>Wed, 28 Feb 2024 09:15:10 +0000</lastBuildDate><itunes:author>Dan Sanchez</itunes:author><itunes:owner><itunes:name>Dan Sanchez</itunes:name><itunes:email>feeds@spreaker.com</itunes:email></itunes:owner><itunes:image href="https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg"/><itunes:subtitle>On Life Sciences Accelerated, we discuss experiences and innovations in compliance and technology from molecule to market. 

Tune in for in-depth interviews with well-known thought leaders, and renowned subject matter experts, with unparalleled...</itunes:subtitle><itunes:summary><![CDATA[On Life Sciences Accelerated, we discuss experiences and innovations in compliance and technology from molecule to market. <br /><br />Tune in for in-depth interviews with well-known thought leaders, and renowned subject matter experts, with unparalleled knowledge in the technology and life sciences industry.   <br /><br />We feature insightful stories that are sure to provide valuable proven new ways to connect technology, people, and data that will take your regulated business to the next level. <br /><br />Episodes will feature topics such as: Digital Transformation, IT Consulting, Pharmaceutical Compliance,  Biotech Compliance, Medical Device Compliance, and more!<br /><br />Innovative, Helpful, and thought-provoking. This is… Life Sciences Accelerated<br /><br />For more information visit, <a href="http://www.usdm.com" rel="noopener">www.usdm.com</a>.]]></itunes:summary><itunes:category text="Science"><itunes:category text="Life Sciences"/></itunes:category><itunes:category text="Business"/><itunes:explicit>false</itunes:explicit><podcast:guid>3c728e66-1cf1-5fe2-af17-245dfdf81595</podcast:guid><itunes:type>episodic</itunes:type><item><title>5: Regulated Workloads in the Public Cloud w/ Vishal Sharma and John Petrakis</title><link>https://www.spreaker.com/episode/5-regulated-workloads-in-the-public-cloud-w-vishal-sharma-and-john-petrakis--51917227</link><description><![CDATA[On this episode of Life Sciences Accelerated, we invited USDM’s Vishal Sharma, VP of Digital Transformation, and John Petrakis, VP of Cloud Assurance, to talk about how to manage your regulated GxP workloads in the public cloud. John holds 30 years of global industry experience in business transformation, delivering solutions that address regulatory and quality pressures. He’s led all aspects of strategy development, delivering value for pharma, biotech, medical device, and healthcare companies. Vishal has spent more than 20 years in life sciences, developing core competencies using emerging technologies to help customers fast-track their digital transformation and achieve high-impact business outcomes.  What we discussed:  The transition from on-premises technologies to the cloud How cloud computing evolved from traditional IT to new service models How regulatory requirements have affected the adoption of newer technologies New things to do with tech like Microsoft Azure, Google Cloud Platform, and AWS Advice for life science companies considering moving to the public cloud  Find this interview and many more by subscribing to Life Sciences Accelerated, on  Apple Podcasts,  Spotify, or our website.]]></description><guid isPermaLink="false">0e1770e9-7824-4235-86ae-ca297c8a2af9</guid><pubDate>Sun, 04 Oct 2020 23:34:39 +0000</pubDate><enclosure url="https://dts.podtrac.com/redirect.mp3/api.spreaker.com/download/episode/51917227/audio_99919_9738_18747_73b58bd1_c880_480c_9e37_0a845749079e.mp3" length="36494149" type="audio/mpeg"/><podcast:transcript url="https://transcription.spreaker.com/sounder/518dcb5e-67be-427d-8572-66c85144e599/518dcb5e-67be-427d-8572-66c85144e599.srt" type="application/x-subrip" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/518dcb5e-67be-427d-8572-66c85144e599/518dcb5e-67be-427d-8572-66c85144e599.txt" type="text/plain" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/518dcb5e-67be-427d-8572-66c85144e599/518dcb5e-67be-427d-8572-66c85144e599.vtt" type="text/vtt" language="en"/><itunes:author>Dan Sanchez</itunes:author><itunes:subtitle>On this episode of Life Sciences Accelerated, we invited USDM’s Vishal Sharma, VP of Digital Transformation, and John Petrakis, VP of Cloud Assurance, to talk about how to manage your regulated GxP workloads in the public cloud. John holds 30 years of...</itunes:subtitle><itunes:summary><![CDATA[On this episode of Life Sciences Accelerated, we invited USDM’s Vishal Sharma, VP of Digital Transformation, and John Petrakis, VP of Cloud Assurance, to talk about how to manage your regulated GxP workloads in the public cloud. John holds 30 years of global industry experience in business transformation, delivering solutions that address regulatory and quality pressures. He’s led all aspects of strategy development, delivering value for pharma, biotech, medical device, and healthcare companies. Vishal has spent more than 20 years in life sciences, developing core competencies using emerging technologies to help customers fast-track their digital transformation and achieve high-impact business outcomes.  What we discussed:  The transition from on-premises technologies to the cloud How cloud computing evolved from traditional IT to new service models How regulatory requirements have affected the adoption of newer technologies New things to do with tech like Microsoft Azure, Google Cloud Platform, and AWS Advice for life science companies considering moving to the public cloud  Find this interview and many more by subscribing to Life Sciences Accelerated, on  Apple Podcasts,  Spotify, or our website.]]></itunes:summary><itunes:duration>2280</itunes:duration><itunes:explicit>false</itunes:explicit><itunes:image href="https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg"/><itunes:episodeType>full</itunes:episodeType></item><item><title>4: GxP Content and Document Management Best Practices w/ Vishal Sharma and Manu Vohra</title><link>https://www.spreaker.com/episode/4-gxp-content-and-document-management-best-practices-w-vishal-sharma-and-manu-vohra--51917225</link><description><![CDATA[On this episode of Life Sciences Accelerated, we invited Vishal Sharma, the VP of Digital Transformation at USDM, and Manu Vohra, the Managing Director of Life Sciences at Box, to talk about content and document management in life sciences. Vishal develops core competencies using emerging technologies to help customers fast-track their digital transformation and achieve high-impact business outcomes. Manu deploys content management solutions for life sciences while running operations within several IT functions supporting drug discovery to commercialization. What we discussed:  Why content management is different for regulated companies Evolution of content management in the life sciences How to manage cloud compliance How Unify Cloud Compliance addresses life science business needs  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></description><guid isPermaLink="false">0db0d486-8180-45c0-8955-f0845de5a30c</guid><pubDate>Tue, 25 Aug 2020 22:03:21 +0000</pubDate><enclosure url="https://dts.podtrac.com/redirect.mp3/api.spreaker.com/download/episode/51917225/audio_99920_9738_18747_315a142a_f96d_4220_9ca0_b8db1cc73764.mp3" length="18899506" type="audio/mpeg"/><podcast:transcript url="https://transcription.spreaker.com/sounder/b38b9998-c92f-410a-9204-8f3d346c9617/b38b9998-c92f-410a-9204-8f3d346c9617.srt" type="application/x-subrip" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/b38b9998-c92f-410a-9204-8f3d346c9617/b38b9998-c92f-410a-9204-8f3d346c9617.txt" type="text/plain" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/b38b9998-c92f-410a-9204-8f3d346c9617/b38b9998-c92f-410a-9204-8f3d346c9617.vtt" type="text/vtt" language="en"/><itunes:author>Dan Sanchez</itunes:author><itunes:subtitle>On this episode of Life Sciences Accelerated, we invited Vishal Sharma, the VP of Digital Transformation at USDM, and Manu Vohra, the Managing Director of Life Sciences at Box, to talk about content and document management in life sciences. Vishal...</itunes:subtitle><itunes:summary><![CDATA[On this episode of Life Sciences Accelerated, we invited Vishal Sharma, the VP of Digital Transformation at USDM, and Manu Vohra, the Managing Director of Life Sciences at Box, to talk about content and document management in life sciences. Vishal develops core competencies using emerging technologies to help customers fast-track their digital transformation and achieve high-impact business outcomes. Manu deploys content management solutions for life sciences while running operations within several IT functions supporting drug discovery to commercialization. What we discussed:  Why content management is different for regulated companies Evolution of content management in the life sciences How to manage cloud compliance How Unify Cloud Compliance addresses life science business needs  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></itunes:summary><itunes:duration>1181</itunes:duration><itunes:explicit>false</itunes:explicit><itunes:image href="https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg"/><itunes:episodeType>full</itunes:episodeType></item><item><title>3: Global UDI and EU MDR Requirements w/ Jay Crowley</title><link>https://www.spreaker.com/episode/3-global-udi-and-eu-mdr-requirements-w-jay-crowley--51917224</link><description><![CDATA[Jay spent 26 years at the FDA, and he developed the requirements for the FDA's UDI system and was one of the authors of the US UDI rule. Jay explains what the delay of enforcement for some class I devices in the US means. Jay Crowley, VP and UDI Practice Lead at USDM Life Science What we talked about:  What are the details of the new UDI and MDR requirements  Determining your organization's requirements Strategies to implement adapted practices  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></description><guid isPermaLink="false">1f0acf0c-4bcd-4cc4-8d20-bf8374f920eb</guid><pubDate>Fri, 31 Jul 2020 19:15:23 +0000</pubDate><enclosure url="https://dts.podtrac.com/redirect.mp3/api.spreaker.com/download/episode/51917224/audio_99921_9738_18747_5519a0ef_6803_4252_b2a2_2e1c01751ff4.mp3" length="14289476" type="audio/mpeg"/><podcast:transcript url="https://transcription.spreaker.com/sounder/3371a13f-bd05-4f0f-ac54-e0cdbd43db66/3371a13f-bd05-4f0f-ac54-e0cdbd43db66.srt" type="application/x-subrip" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/3371a13f-bd05-4f0f-ac54-e0cdbd43db66/3371a13f-bd05-4f0f-ac54-e0cdbd43db66.txt" type="text/plain" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/3371a13f-bd05-4f0f-ac54-e0cdbd43db66/3371a13f-bd05-4f0f-ac54-e0cdbd43db66.vtt" type="text/vtt" language="en"/><itunes:author>Dan Sanchez</itunes:author><itunes:subtitle>Jay spent 26 years at the FDA, and he developed the requirements for the FDA's UDI system and was one of the authors of the US UDI rule. Jay explains what the delay of enforcement for some class I devices in the US means. Jay Crowley, VP and UDI...</itunes:subtitle><itunes:summary><![CDATA[Jay spent 26 years at the FDA, and he developed the requirements for the FDA's UDI system and was one of the authors of the US UDI rule. Jay explains what the delay of enforcement for some class I devices in the US means. Jay Crowley, VP and UDI Practice Lead at USDM Life Science What we talked about:  What are the details of the new UDI and MDR requirements  Determining your organization's requirements Strategies to implement adapted practices  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></itunes:summary><itunes:duration>893</itunes:duration><itunes:explicit>false</itunes:explicit><itunes:image href="https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg"/><itunes:episodeType>full</itunes:episodeType></item><item><title>2: Cloud-Based Systems in Life Sciences w/ David Blewitt</title><link>https://www.spreaker.com/episode/2-cloud-based-systems-in-life-sciences-w-david-blewitt--51917226</link><description><![CDATA[He's an accomplished life sciences, regulatory and ISDN compliance professional. With more than 25 years of experience in the pharmaceutical medical device, biotech and blood management industries, specifically in the fields of computer systems, validation, risk management, and quality assurance, software development, product, life cycle management, and compliance roadmap development. David Blewitt, Vice President of Cloud Compliance, USDM Life Sciences What we talked about:  Cloud usage in Life Sciences New applications for usage Adapting to conducting business in a COVID 19 environment  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></description><guid isPermaLink="false">36cbb691-2df8-45df-baa5-41dfe2efa7a7</guid><pubDate>Fri, 31 Jul 2020 19:13:52 +0000</pubDate><enclosure url="https://dts.podtrac.com/redirect.mp3/api.spreaker.com/download/episode/51917226/audio_99922_9738_18747_6ae26fec_585a_4ae6_a1db_afe9a35e5ddb.mp3" length="22857117" type="audio/mpeg"/><podcast:transcript url="https://transcription.spreaker.com/sounder/be338ca8-b716-4782-b1c8-67f5a8ff71cd/be338ca8-b716-4782-b1c8-67f5a8ff71cd.srt" type="application/x-subrip" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/be338ca8-b716-4782-b1c8-67f5a8ff71cd/be338ca8-b716-4782-b1c8-67f5a8ff71cd.txt" type="text/plain" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/be338ca8-b716-4782-b1c8-67f5a8ff71cd/be338ca8-b716-4782-b1c8-67f5a8ff71cd.vtt" type="text/vtt" language="en"/><itunes:author>Dan Sanchez</itunes:author><itunes:subtitle>He's an accomplished life sciences, regulatory and ISDN compliance professional. With more than 25 years of experience in the pharmaceutical medical device, biotech and blood management industries, specifically in the fields of computer systems,...</itunes:subtitle><itunes:summary><![CDATA[He's an accomplished life sciences, regulatory and ISDN compliance professional. With more than 25 years of experience in the pharmaceutical medical device, biotech and blood management industries, specifically in the fields of computer systems, validation, risk management, and quality assurance, software development, product, life cycle management, and compliance roadmap development. David Blewitt, Vice President of Cloud Compliance, USDM Life Sciences What we talked about:  Cloud usage in Life Sciences New applications for usage Adapting to conducting business in a COVID 19 environment  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></itunes:summary><itunes:duration>1428</itunes:duration><itunes:explicit>false</itunes:explicit><itunes:image href="https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg"/><itunes:episodeType>full</itunes:episodeType></item><item><title>1: Adapting Computer System Validation to Accommodate Evolving FDA Guidance w/ Diane Gleinser and Sandy Hedberg</title><link>https://www.spreaker.com/episode/1-adapting-computer-system-validation-to-accommodate-evolving-fda-guidance-w-diane-gleinser-and-sandy-hedberg--51917223</link><description><![CDATA[As the Life Sciences adapt to manufacturing amidst Covid-19, the FDA is also updating guidelines for computer system validation. So, what does this mean for your organization? Diane Gleinser and Sandy Hedberg discuss the intricacies of the new guidance, and how you will need to adapt when it comes to showing evidence that the computer systems you're using comply with the predicate rules.   Diane has an impressive background in the Life Sciences, and brings her experience, knowledge, and her certification in medical device and pharmaceutical law to USDM and the industry as a whole. Diane Gleisner , VP Life Science Services and Solutions Sandy Hedberg QA/RA Manager, Cloud Assurance at USDM Life Sciences USDM Life Sciences What we talked about:  Changes coming to Computer System Validation The FDA’s urging company’s to utilize automation in their manufacturing process  CSA approach vs CSV  approach  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></description><guid isPermaLink="false">81fdd236-91bb-49e9-b624-52fa4e4cfc7e</guid><pubDate>Fri, 31 Jul 2020 19:09:42 +0000</pubDate><enclosure url="https://dts.podtrac.com/redirect.mp3/api.spreaker.com/download/episode/51917223/audio_99923_9738_18747_79926427_a665_49a7_8ed8_3e178b67f52a.mp3" length="21652024" type="audio/mpeg"/><podcast:transcript url="https://transcription.spreaker.com/sounder/2f3ba007-7742-42a4-8d54-df780a3ce437/2f3ba007-7742-42a4-8d54-df780a3ce437.srt" type="application/x-subrip" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/2f3ba007-7742-42a4-8d54-df780a3ce437/2f3ba007-7742-42a4-8d54-df780a3ce437.txt" type="text/plain" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/2f3ba007-7742-42a4-8d54-df780a3ce437/2f3ba007-7742-42a4-8d54-df780a3ce437.vtt" type="text/vtt" language="en"/><itunes:author>Dan Sanchez</itunes:author><itunes:subtitle>As the Life Sciences adapt to manufacturing amidst Covid-19, the FDA is also updating guidelines for computer system validation. So, what does this mean for your organization? Diane Gleinser and Sandy Hedberg discuss the intricacies of the new...</itunes:subtitle><itunes:summary><![CDATA[As the Life Sciences adapt to manufacturing amidst Covid-19, the FDA is also updating guidelines for computer system validation. So, what does this mean for your organization? Diane Gleinser and Sandy Hedberg discuss the intricacies of the new guidance, and how you will need to adapt when it comes to showing evidence that the computer systems you're using comply with the predicate rules.   Diane has an impressive background in the Life Sciences, and brings her experience, knowledge, and her certification in medical device and pharmaceutical law to USDM and the industry as a whole. Diane Gleisner , VP Life Science Services and Solutions Sandy Hedberg QA/RA Manager, Cloud Assurance at USDM Life Sciences USDM Life Sciences What we talked about:  Changes coming to Computer System Validation The FDA’s urging company’s to utilize automation in their manufacturing process  CSA approach vs CSV  approach  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.]]></itunes:summary><itunes:duration>1353</itunes:duration><itunes:explicit>false</itunes:explicit><itunes:image href="https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg"/><itunes:episodeType>full</itunes:episodeType></item><item><title>Life Sciences Accelerated: A brand new podcast for the Life Sciences industry w/ Ryan Carmel</title><link>https://www.spreaker.com/episode/life-sciences-accelerated-a-brand-new-podcast-for-the-life-sciences-industry-w-ryan-carmel--51917222</link><description><![CDATA[7 year Life Sciences industry veteran, Ryan Carmel, Marketing Director at USDM, will host a brand new podcast bringing relevant and educational peer content to the people within the life sciences industry. Well versed in the unique business challenges, and more recently helping organizations with the immediate need to fast-track their digital transformation in light of COVID-19, USDM has become a trusted advisor to many regulated pharma, medical device, and biotech firms, and now, cannabis companies.  With 20 years of consulting in this space, USDM Life Sciences’ depth of regulatory and FDA expertise this podcast will provide a new, more modern forum to tell stories and share lessons learned, helping life sciences companies with their challenges. What we talked about:  Launching “Life Sciences Accelerated” w/ host Ryan Carmel Regulatory and FDA consulting expertise  Unique business challenges in the Life Sciences industry  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.   ]]></description><guid isPermaLink="false">735ad760-fb08-4a6f-9f2e-5b1c7b660b84</guid><pubDate>Fri, 03 Jul 2020 03:05:55 +0000</pubDate><enclosure url="https://dts.podtrac.com/redirect.mp3/api.spreaker.com/download/episode/51917222/audio_99924_9738_18747_c743bf3b_5897_46a2_98e2_d93eb703e245.mp3" length="7926455" type="audio/mpeg"/><podcast:transcript url="https://transcription.spreaker.com/sounder/ba35a735-82f8-4c5f-883c-5d85a4213f7e/ba35a735-82f8-4c5f-883c-5d85a4213f7e.srt" type="application/x-subrip" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/ba35a735-82f8-4c5f-883c-5d85a4213f7e/ba35a735-82f8-4c5f-883c-5d85a4213f7e.txt" type="text/plain" language="en"/><podcast:transcript url="https://transcription.spreaker.com/sounder/ba35a735-82f8-4c5f-883c-5d85a4213f7e/ba35a735-82f8-4c5f-883c-5d85a4213f7e.vtt" type="text/vtt" language="en"/><itunes:author>Dan Sanchez</itunes:author><itunes:subtitle>7 year Life Sciences industry veteran, Ryan Carmel, Marketing Director at USDM, will host a brand new podcast bringing relevant and educational peer content to the people within the life sciences industry. Well versed in the unique business...</itunes:subtitle><itunes:summary><![CDATA[7 year Life Sciences industry veteran, Ryan Carmel, Marketing Director at USDM, will host a brand new podcast bringing relevant and educational peer content to the people within the life sciences industry. Well versed in the unique business challenges, and more recently helping organizations with the immediate need to fast-track their digital transformation in light of COVID-19, USDM has become a trusted advisor to many regulated pharma, medical device, and biotech firms, and now, cannabis companies.  With 20 years of consulting in this space, USDM Life Sciences’ depth of regulatory and FDA expertise this podcast will provide a new, more modern forum to tell stories and share lessons learned, helping life sciences companies with their challenges. What we talked about:  Launching “Life Sciences Accelerated” w/ host Ryan Carmel Regulatory and FDA consulting expertise  Unique business challenges in the Life Sciences industry  Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.   ]]></itunes:summary><itunes:duration>495</itunes:duration><itunes:explicit>false</itunes:explicit><itunes:image href="https://d3wo5wojvuv7l.cloudfront.net/t_rss_itunes_square_1400/images.spreaker.com/original/3dfc26c4737c38fb94d4ccdc125a1577.jpg"/><itunes:episodeType>full</itunes:episodeType></item></channel></rss>
