4.2.2026 | EU Medical Device Regulation (MDR and IVDR): Latest Developments and Expert Analysis
Tapahtuman tiedot
Ajankohta
The Commission has published a proposal on major changes to the MDR and IVDR. Come and hear the latest analysis of the suggested changes in EU regulation, discussion led by Erik Vollebregt and Nelli Karhu.
Feedback on the regulations for medical devices and IVDs in the EU has been collected by the Commission during 2025 and there is great political pressure for change. We will hear experts’ views on the ongoing regulatory changes freshly.
In addition to presentations, there will be plenty of time for discussion and questions.
Speakers (to be finalised in January)
Erik Vollebregt, partner, Axon Lawyers
Ajda Mihelčič, Director of Technical & Regulatory Affairs, COCIR
with participation from the Ministry of Health and Fimea
The detailed programme and list of speakers will be completed in early 2026.
The event will take place on 4 February 2026 in Helsinki, just preceding Labquality Days, so participation in both events can be conveniently combined. The event will be hybrid, with a limited number of seats at Eteläranta. Please remember to specify whether you will attend remotely or on-site and remember to inform us if you change plans regarding on-site participation.
You can also meet Erik and Ajda at Labquality Days. If you would like to meet up with Ajda and perhaps introduce your company, please contact Nelli or Päivi.
The event is for HealthTech Finland members and separately invited guests – we may open up registration for others on 30.1.2026 if there is room.
Link for the registration: contact Nelli or Päivi.
