Jana Russo

Jana joined MedTech Europe in May 2018 and currently leads the Medical Devices Regulation implementation for Labelling and Implant Cards, Procedure Packs, Borderline& Classification and Economic Operators (IVD and MD). She also supports her colleagues in Post Market Surveillance and Clinical Investigations work. In 2021 Jana added Software (IVD and MD) to her portfolio. In April 2026, Jana Russo became Senior Expert Medical Devices.

Jana’s goal is to provide MedTech Europe members with a high-quality support and expertise in order to facilitate the MDR implementation.

Jana has 7 years of experience in the EU public affairs, including health policy, patient advocacy and extensive member interface. She is a graduate of the University of Edinburgh and speaks fluently English, Spanish, Italian and Czech.

Outside of work, Jana is a passionate gardener and works on improving her French.