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MedTech Europe’s reaction to the European Commission proposal to amend the in vitro diagnostics medical device and medical devices regulations

Posted on 01.02.2024

With its statement, MedTech Europe acknowledges the European Commission proposal for extending the In Vitro Diagnostic Medical Devices Regulation (IVDR) transitional periods, and – for both the IVD Regulation and Medical Devices Regulation – allowing for early mandatory use of European medical devices database (EUDAMED) modules and requiring notification of device discontinuations.

MedTech Europe supports any measures that keep devices available to the patients who need them. The additional time given under the IVDR must be used by the European Commission, Medical Devices Coordination Group (MDCG), Notified Bodies, and other actors to identify blockages and rectify existing issues, to enable all manufacturers to transition on time and meet post-market requirements. In that regard, MedTech Europe welcomes the European Commission’s announcement to start preparatory work for a targeted evaluation of the legislation in 2024, in addition to taking more immediate actions. The integrity of the EUDAMED database and its practical implementation are essential for ensuring the success of a mandatory EUDAMED.

The proposed amendments should avoid creating additional financial implications for device manufacturers and should be accompanied by guidance to support the smooth implementation of the proposed amendments as soon as possible.

Discussions between all stakeholders must continue in 2024 to implement lasting solutions to improve efficiency, foster innovation and improve governance, in order to make the Regulations truly work for patients and European health systems.

For more information, please contact Petra Zoellner, Director Regulatory Affairs (IVDR & MDR).

For more information, please contact Alice Bova, Officer In Vitro Diagnostics.