Recording of the 1^st S3martMed Webinar – March 13^th 2019 – from 14:00 to 15:00

The first webinar of the S3martMed project was held on March 13th 2019. This was dedicated to a crucial topic for European Medtech companies: “Implementation insights of the new European Regulation on Medical Devices (MDR)”. One expert Mr. Martin Witte, Global Director of Active Medical Implants, TÜV SÜD Product Service GmbH ​provided the key facts on the new MDR.

Here is the recorded session.