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MedTech Europe Survey on MDR implementation Background and More information


April 2022
Since 26 May 2021, the Medical Devices Regulation (MDR) has come into full application. An overwhelming majority of MedTech Europe members are reporting challenges with the MDR implementation.


Within the framework of our new MDR advocacy efforts, MedTech Europe and its members have identified priority areas that lead to an unpredictable and innovation unfriendly European regulatory system, e.g., challenges when transitioning Directive certificates, lack of notified body capacity, fragmented MDR implementation across Europe, implementation of guidelines, innovation, etc. We now need concrete evidence and data to illustrate these points and with that in mind, we are reaching out to you with a request to fill in a survey by 25 April 2022 (EOB).



MORE INFORMATIONCheck the survey