The European Commission is hosting a free hybrid workshop in Stuttgart to support onboarding to EUDAMED, the EU’s database for medical devices. The event will guide stakeholders—such as economic operators, notified bodies, and national authorities—on meeting their obligations under the MDR and IVDR, particularly regarding EUDAMED’s mandatory modules (Actors, UDI/Devices, Notified Bodies and Certificates, Market Surveillance).
Additional workshops with identical content will be held in Rome (8 October) and Brussels (3 December), with online streaming available for all sessions.
Registration for Stuttgart closes on 5 May (physical) and 12 May (online), with priority for certain Central European countries. Rome and Brussels registration will open later.
The workshop aims to clarify EUDAMED’s functionality, timelines, and integration into regulatory compliance.
To register for this workshop, please use the following link
