Medical Devices Regulation (MDR) implementation – MedTech Europe Survey
Since 26 May 2021, the Medical Devices Regulation (MDR) has come into full application. Within the framework of new MDR advocacy efforts, MedTech Europe and its members have identified priority areas that lead to an unpredictable and innovation unfriendly regulatory system. These include e.g. challenges when transitioning Directive certificates, lack of Notified Body capacity, fragmented […]