Master EU MDR & IVDR vigilance complexities with Veronika Valdova
Tough Questions: Mastering Post-Market Surveillance
Welcome to our in-depth panel discussion on the critical aspects of regulatory obligations and risk management in the medical device industry. In this video, we dive into the complexities of postmarket surveillance in both the EU and US, exploring key topics such as predicate selection, biological safety, and more.
Join our distinguished panelists—Martin King, Sean Smith, Marina Daineko, Karandeep Singh Badwal, Michelle Lott, and Ajda Mihelčič—as they tackle the tough questions and share their valuable insights. Prepare to gain a deeper understanding of how to navigate the evolving regulatory landscape and ensure compliance.
Featuring an All-Expert Panel:
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Karandeep Singh Badwal, QRA Medical
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Marina Daineko, Intrinsic Medical Group
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Michelle Lott, RAC, Lean RAQA
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Ajda Mihelčič, Obellis Group
Special Bonus Insights:
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EU MDR Compliance: Access our free Postmarket Surveillance (PMS) guide.
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Notified Body PMS Tips: Enjoy exclusive interviews with Marta Carnielli and Tom Patten.