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  <title>Medical Device Regulation, Compliance &amp;amp; Policy, Part 2: A Look at Europe &amp;amp; China</title>
  <description> In this second part of our series in collaboration with Covington, Wayne chats with Sarah Cowlishaw, Partner in Covington’s European Food, Drug and Device Practice; John Balzano, Partner in Covington’s China Food, Drug and Device Practice; and Julia Post, Of Counsel in Covington’s U.S. and China Food, Drug and Device Practices. Together, they discuss the top issues in the global device landscape; developments in the European and Chinese medical device spaces; cross-border access to and transfers of U.S. and Chinese data and biospecimens; how Europe and China are approaching digital health and AI in device regulation; what device companies doing business in the U.S., European Union and China should be watching for over the next year; and much more.  This episode and the rest of our series do not include the usual Headlines and Resources Links segments.  To subscribe or find out more information about our podcast, visit  FDAWatch.net.  Want to be a sponsor, marketing partner, or guest, or provide feedback on the podcast? Email us at  info@fdawatch.net.&amp;amp;nbsp;  Music by   Dvir Silver  from   Pixabay. </description>
  <author_name>FDA Watch</author_name>
  <author_url>https://sites.libsyn.com/557121</author_url>
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