R&Q's Blog

Medical device industry news and trends - and the resources to understand and act on them.


Not your average EU MDR and CER workshop


Note: Presenters/Panelists listed below subject to change.

DeviceTalks Boston is Oct. 8-10 this year and as part of it, R&Q is helping to organize an Advanced EU MDR and CER Workshop. It's an extensive, 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. They've seen what works... and what doesn't, and will be sharing tips, tricks, and lessons learned.

At a small company and think this doesn't apply yet? This may not be on your radar, but it should be. You'll learn from the successes and failures of larger companies who are several months into the transition, and acquire the knowledge to nimbly navigate the transition efficiently. If your organization has many device changes planned, it’s crucial to get started in order to complete the transition by May 2020.

Read on for a closer look at the workshop and an exclusive registration discount code for DeviceTalks Boston.

🔑 Unlock the Secrets to CERs in our May Webinar


Unlock the secrets to complying with the increased requirements for CERs in May's free R&Q webinar:


CERs – Tips, Tricks, and Lessons Learned


Sign Up


The session will be on Tuesday, May 22 from 1:00pm - 2:00pm EST. The presentation slides, webinar recording, and Q&A will be made available to registrants - whether you can attend the live presentation or not.


Webinar details

You have heard about the increased requirements for clinical evaluation with MEDDEV 2.7/1 Rev 4 and the MDR. You may be working on new templates and updating your CERs.


And now come the questions...

  • What do these requirements really mean?
  • Why are we doing this?
  • How are we going to get this all done?


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