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.

Welcome to MedTech ON AIR, the new podcast by MedTech Europe, the European trade association for the medical technology industry.

Together with experts in the field, we will explore the world of medical technology, touching on the most pressing issues that are affecting the industry, healthcare systems, and society.

Tune in from January 2020 and join us for the start of our journey.