ABHI Response: EU Call for Evidence on MDR & IVDR Revision
Topic : Position Papers Type : Consultation Response
The ABHI response to the European Commission’s call for evidence on the targeted revision of the Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulation (IVDR) can be found here.
We prepared this combined submission reflecting member inputs and priorities, and as ever, we thank our Members for their contribution to this work.