Date: 28 October, 2026
Location: De Kloosterhoeve, Harmelen, Utrecht, The Netherlands
Introduction:
How do developments in medical device regulation and standardization translate into everyday practice? Join the MDR Symposium to explore this question with professionals from the medical device industry, healthcare institutions, and more. The symposium will examine the evolving Medical Device Regulation (MDR), from developments in Brussels and the revision of the MDR to EUDAMED, the practical role of standards and the growing use of AI in healthcare.
Gert Bos will chair the symposium, opening the day with a welcome and guiding participants through the dialogue tables and their key takeaways. Qserve’s Bianca Lutters, Head of Clinical Affairs, will also contribute to the dialogue table on Clinical Data. To round off the day, Gert will moderate the panel discussion, “Making Sense of the MDR Transition Together,” discussing the current developments and the impact of MDR revisions in practice, before delivering the closing remarks.
Through presentations, discussions and workshops, participants will gain insight into the latest developments and explore what they mean for their organizations. Connect with professionals across the sector, exchange perspectives and deepen your understanding of how regulation and standardization work together in practice.
For more details, the full agenda, and speaker overview, visit the event website.