Join regulatory colleagues from your region for an evening of networking and an expert presentation on the EU Medical Device Regulation.
Medical device manufacturers are facing major changes in the EU regulatory framework that oversees market access to Europe. This presentation will provide an overview of the draft MDR, including highlights of the Notified Bodies designation process, expected transition timelines and chapters and annexes of the regulation. You’ll come away with 10 key steps to successful certification.
This meeting is sponsored by the RAPS Wisconsin Chapter and is intended to promote knowledge advancement and facilitate networking among local regulatory and quality professionals. A light meal will be available. RAC holders can claim one RAC recertification credit.