MDR & IVDR: Have your say!

The European Commission has launched a public consultation and call for evidence on the European Regulation on medical devices and in vitro diagnostic medical devices. The aim of this initiative is to assess the effectiveness of the current rules and identify possible areas for improvement. Stakeholders can share their views on costs, administrative burden, and impact on the availability of devices, including “orphan devices”.

The consultation is open until March 21, 2025. Take part and make your voice heard to shape a regulatory framework that supports innovation while guaranteeing patient safety!

HAVE YOUR SAY