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Training on the Medical Device Regulation

On April 17th, 2018, ICRC-Weyer attended the 47th session of the Medical Device Regulation (MDR) Workgroup, hosted by the German Society of Pharmaceutical Medicine (DGPharMed) in Berlin. The meeting focused on the regulatory challenges the Medical Device Industry will face in the coming years as a result of EU regulation 2017/745, which entered into force on May 25th 2017. In the ever evolving regulatory landscape, it is of utmost importance that Medical Device manufacturers familiarize themselves with the new rules well in advance of Spring 2020, when the transition period will be complete, and the legislation will become legally binding in all EU member states.

ICRC-Weyer will remain the trusted partner for the Medical Device Industry, providing regulatory consulting and turnkey solutions both during the transition period and beyond.

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