The Medical Device Coordination Group (MDCG), made up of representatives of the Member States and chaired by the European Commission, announced on Monday 29 August the approval of a list of measures to facilitate the transition to the implementation of the Medical Devices Regulation (Regulation (EU) 2017/745) and the In Vitro Diagnostic Medical Devices Regulation (Regulation (EU) 2017/746).
At the Health Ministers’ meeting on 14 June, Member States expressed concerns about possible...