The five European life science clusters part of the S3martMed ESCP-S3 initiative are happy to invite you to attend the webinar “Key facts on the new European Regulation on Medical Devices”, on March, 13^th, 2019 at 14.00 p.m.

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: altintoprak [at] bioregio-stern.de

Access data will be sent after registration.