This event will be an extensive yet detailed look at EU MDR and CERs through the lens of top industry experts who have successfully implemented large-scale EU MDR programs and completed 100’s of CERs. RA/QA leaders from multinational medical device companies – along with preeminent RA/QA experts from R&Q – will share invaluable tips and lessons learned from seeing what works first-hand… and what doesn’t. You’ll have the opportunity to ask questions throughout the day, and will leave the event with an advanced skillset and developed strategies no matter where you are in the EU MDR transition process.
Please see the agenda breakout for specific detail on each session and we hope to see you at the event!
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