The changing EU regulatory landscape: CE Marking for Medical Technology

The first episode of MedTech ON AIR, the new MedTech Europe podcast, is online. Together with Oliver Bisazza, we discuss new medical technology regulations and their impact on the CE marking process.

Last update on 27.02.2020

Listen to the episode below

The three-year transition period for the new Medical Device Regulation will end on 26 May 2020, and the new In Vitro Diagnostic Regulation will come into force in 2022. These new pieces of legislation bring changes to one of the pillars of the medical technology sector: the CE marking process. In this episode, we speak to Oliver Bisazza about what this process is, how it changes and what the medtech industry has to say about it.

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