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
