Medical Device Update

First Jörg Schickert, Arne Thiermann and Matthias Schweiger took a closer look at the European Medical Device Regulation (MDR), focusing on the economic operators and their external responsibilities, inter-company agreements and supply chain structures. They further discussed the internal distribution of tasks between responsible parties and quality management, and also  had a look on the product safety and product liability context of the MDR. 

In the second part of the webinar Jörg Schickert, Arne Thiermann, Nicole Böck and Martin Pflüger then turned their attention to digitalization and digital medical devices and discuss responsibilities from a regulatory and product liability perspective, the current regulatory framework of artificial intelligence, as well as the topics of cyber security and data protection. Last but not least, Michael Penners gave a short overview of advertising digital medical devices and the legal defence therefore.

Please click here to see a recording of the webinar.

Authored by Jörg Schickert, Arne Thiermann, Mattias Schweiger, Martin Pflüger, Nicole Böck and Michael Penners.