Februar 14, 2025
Regulatory

European Commission Releases New Factsheets

The European Commission has released the updated version of the Factsheet for authorities in non-EU/EEA countries regarding medical devices and in vitro diagnostic medical devices.

The European Commission has released the updated version of the Factsheet for authorities in non-EU/EEA countries regarding medical devices and in vitro diagnostic medical devices. This document aims to provide a comprehensive overview of the transition to the EU Medical Device Regulation and the In Vitro Diagnostic Medical Device Regulation, including revised timelines and conditions that authorities in third countries must meet to benefit from the extended transition periods.

Additionally, updated versions of the Factsheet for the Procurement Ecosystem of medical devices and in vitro diagnostic medical devices, as well as the Factsheet for healthcare professionals and health institutions, have also been published.

 

Source: European Commission