The IMDRF Management Committee (MC) welcomed 350+ professionals to Brussels who participated to the EU chaired sessions as follows:
Day 1: 27 March 2023
Joint IMDRF / Stakeholder (DITTA-GMTA) Workshop
Hear about the most recent developments in the field at this joint regulator-stakeholders session on post-market related activities
Sessions focused on post-market related issues faced in the medical device field and included 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
Hear updates from the IMDRF MC Regulatory Authorities, Official Observers and IMDRF Working Groups
Get updates from the eight IMDRF Working Groups on their work
Hear from IMDRF stakeholders, Regional Harmonisation Initiatives and other interested regulators active in IMDRF
The IMDRF 2023 Secretariat would like to thank you for your participation and hopes to welcome you in Berlin on 25-26 September. Register now!