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Medical devices

 A panel discussion on the EU MDR lessons learned since the May 26th deadline, requiring all new medical devices to meet Regulation (EU) 2017/745. The webinar covers key concerns, challenges and common non-conformities that manufacturers, consultants and notified bodies see from the application stage to final approval.   

EU MDR Lessons Learned

Download the slides for the November 30, 2021 webinar

"EU MDR Lessons Learned" webinar presentation materials

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