The International Medical Device Regulators Forum (IMDRF) sessions will be held in the EU and hosted by the European Commission.

IMDRF is a voluntary group of medical device regulators from around the world who have come together to build on the strong foundational work of the Global Harmonization Task Force on Medical Devices (GHTF) and aims to accelerate international medical device regulatory harmonisation and convergence. 

The IMDRF Management Committee (MC) welcomes you to the EU chaired sessions and encourages you to register to participate in the following activities:

Day 1: 27 March 2023
Joint IMDRF / Stakeholder (DITTA-GMTA) Workshop

• Join us to hear about the most recent developments in the field at this joint regulator-stakeholders session on post-market related activities
• Sessions will focus on post-market related issues faced in the medical device field include burning topics like real-world evidence, vigilance and safety notices and post-market considerations for software and artificial intelligence

Day 2: 28 March 2023
IMDRF Stakeholder Forum

• Join us to hear updates from the IMDRF MC Regulatory Authorities, Official Observers and IMDRF Working Groups
• Don’t miss the updates from the eight IMDRF Working Groups on their work
• Hear from IMDRF stakeholders, Regional Harmonisation Initiatives and other interested regulators active in IMDRF