EUDAMED workshop

The European Commission is organising free hybrid workshops to support the onboarding of all concerned actors to EUDAMED, in preparation for the mandatory use of Actors, UDI/Devices, Notified bodies and Certificates and Market surveillance modules.

The workshop provides an overview of the obligations under the Medical Devices Regulations (Regulation (EU) 2017/745 — MDR, and Regulation (EU) 2017/746 — IVDR). 

These workshops are a good opportunity for economic operators, notified bodies, national authorities, and other stakeholders to prepare for compliance with the Regulations in the context of EUDAMED.

More info and registration at this link