Registration is now open for the EU MDR and IVDR Summit 2026, taking place on 8-9 September in Brussels.
The Summit brings together regulators, competent authorities, notified bodies, authorised representatives, and manufacturers worldwide to examine how the EU provisions for medical devices and IVDs are being applied in practice. The summit will address interpretation gaps, accountability across the value chain and ongoing discussions on the MDR and IVD amendments, including certification timelines, market access, and long-term compliance strategies.
What to expect
For those responsible for regulatory, quality, and EU market access, this is a focused forum to gain clarity on expectations, exchange practical experience, and stay aligned with the direction of the regulatory framework.
In particular, by attending you will gain:
- Understand how MDR/IVDR requirements are applied in practice
- Gain clarity on working with authorised representatives
- Identify gaps in your current compliance approach
- Make more informed, defensible regulatory decisions
Where and when
8-9 September 2026, at Sheraton Brussels Airport Hotel, in Brussels, Belgium.
Early bird pricing ends June 30, 2026.
Register here
