New year, new factsheets

Posted on 06.02.2025

The European Commission has published the new version of the Factsheet for authorities in non-EU/EEA states on medical devices and in vitro diagnostic medical devices. The document aims to provide a high-level overview of the transition to the EU Medical Device Regulation and In Vitro Diagnostic Medical Device Regulation, including reviewed timelines and conditions for authorities in third countries to be fulfilled to benefit from the extended transition periods.

In addition, the updated versions of the Factsheet for Procurement Ecosystem of medical devices and in vitro diagnostic medical devices and of the Factsheet for healthcare professionals and health institutions have also been released.

For more information, please contact Dario Belluomini, Manager International Affairs.