MassMEDIC and Regulatory & Quality Solutions (R&Q) are partnering to bring you an industry-leading EU MDR and CER workshop event in Boston.

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!

The goal of this event is to educate medical device manufacturers and based on limited seating, we are prioritizing registrations first for medical device manufacturers. If seats remain closer to the event date, we will open up registration to service providers and consultants. Please note the different ticket types.

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