MedTech Europe submission to the European Commission’s Call for Evidence consultation on the MDR/IVDR simplification reform

MedTech Europe has submitted its response to the Call for Evidence consultation conducted by the European Commission in the context of the targeted reform of the Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR).

In its response, MedTech Europe reiterated the key advocacy priorities of the medical technology industry and referenced a range of supporting evidence and analyses relevant to the ongoing legislative reforms.

The contribution aims to inform the European Commission’s evaluation process and supports the development of a more efficient, proportionate, and predictable regulatory system for medical technologies in Europe.

Read our full submission below.