Between sessions at the MedTech Forum 2026, we sat down with Flora Giorgio, Head of Unit D3 for Medical Devices at the European Commission’s DG SANTE. In this conversation, we unpack some of the most consequential files in medtech policy right now: from the revision of the Medical Devices Regulation (#MDR) and the In Vitro Diagnostics Regulation (#IVDR), to EUDAMED implementation and the European Commission’s breakthrough pilot.
***
Listen to the episode: https://bit.ly/3QEV1Z0
Posted on 03.06.2026
From our booth at The MedTech Forum 2026, we sat down with Prof. Marc Peeters, Professor of Oncology at the University of Antwerp and board member of AZ Maria Middelares and Ziekenhuis Geel. We discussed today’s challenges and opportunities in medtech, and AI emerged as a clear leitmotif throughout the conversation. Timely, as discussions on […]
The MDR/IVDR revision marks a pivotal moment for the EU medtech sector. Read MedTech Europe's full position on the revision.
