Medical device update for the German market Part II


The regulatory environment in the medical device sector is evolving constantly. New legislation is being passed, new challenges require a closer legal assessment, new technologies are changing demands in many aspects. The ongoing global pandemic has disrupted the industry and created a legal threshold for medical devices in this specific area of the industry. The German market has some challenges that need to be taken into account when planning to bring a product to market. Therefore, the German Life Sciences and Health Care team annually offers a broad overview of the most important changes and new developments in this market.

Please join us for our first English edition of the medical device update for the German market on Wednesday, 27 January and 3 February 2021 each starting at 5:00 p.m. CET. After part one we invite all attendees to join us for a virtual get-together.

In part two of the webinar series, we will discuss the legal aspects of self-tests/kits and laboratory diagnostics - from covid to gene analysis. Our event will be rounded off by a presentation on inter-company agreements between different economic operators under the MDR.

Please find the agenda here.

Click here to register for this event

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