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TÜV Rheinland Italia participates to the session 2 of the webinar “26 MAY 2021: WE ARE STARTED! THE NEW EUROPEAN REGULATION CHALLENGES AND OPPORTUNITIES ”of AFI

12.10.2021Pogliano Milanese (MI)

The Scientific Sessions of AFI, the Association of Pharmaceuticals Industry Scientific Society, continue in webinar mode.

Five months after the entry into force of the European Regulation 2017/745 of Medical Devices, a "round table" was organized to discuss in particular the clinical data necessary to support the certification in MDR and to tell the first experiences and try to clarify the doubts and uncertainties that still remain regarding the new regulatory horizon.

The event will be attended by Manufacturers, Competent Authorities and Notified Bodies, including TÜV Rheinland Italia, represented by Cesare Gentile, Technical Manager of the medical sector, during the round table with the Notified Bodies from 15.45 to 16.45.

The event will take place on October 14, 2021, live on the web, from 14.00 to 17.00.

For more information and registration, please click here.