Medical Device Update

In this years Medical Device Update, we will first take a closer look at the European Medical Device Regulation (MDR)

In this years Medical Device Update, we will first take 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. We will also discuss the internal distribution of tasks between responsible parties and quality management. Finally, there will be a brief update on product safety and product liability in the context of the MDR. 

Our speakers will then turn 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, as well as advertising of digital medical devices and legal defence.

Download the agenda here.


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