The webinar aims to offer support to the SMEs working in the field of medical technology that are being affected by the implementation of the new European Medical Device Regulation (MDR).
Agenda – Key facts on the European Regulation on Medical Devices
- 14.00 – Welcome, Introduction of the „S3martMed“ project. by Mélanie Denizot, Lyonbiopole (Auvergne-Rhône-Alpes);
- 14.10 – Key facts on the new MDR – focus on the main changes and innovations. by Martin Witte, Global Director of Active Medical Implants, TÜV SÜD Product Service GmbH;
- 14.55 – Q & A
In order to participate, please register by writing to: firstname.lastname@example.org.
Access data will be sent after registration.