MINI-SYMPOSIUM on medical devices: European regulations in the spotlight – MDR and GDPR

European legislation is leading to more and more regulatory requirements being set out for manufacturers of medical devices. In this respect, two regulations are currently key: GDPR, since May 2018, and the new MDR, from May 2020. What is the current situation and what measures need to be implemented as a matter of urgency?

In our MINI-SYMPOSIUM, we deal with questions from a variety of perspectives. Participants are invited to discuss the content with our expert speakers.