Berlin, Germany (hosted by European Commission on behalf of the EU)
Jurisdictional Updates
Australia (TGA)
Brazil
Canada
China
European Union
Japan
Singapore
South Korea
United Kingdom
United States of America
Argentina
Switzerland
WHO
Working Group Updates
Adverse Event Terminology Working Group
Artificial Intelligence/Machine Learning-enabled Working Group
Quality Management Systems Working Group
Regulated Product Submission Working Group
Software as a Medical Device Working Group
Personalized Medical Devices Working Group
Good Regulatory Review Practices Working Group
Medical Device Cybersecurity Guide Working Group
Stakeholder Updates
APEC
GHWP
DITTA
GMTA
AMDF
Joint IMDRF/DITTA and GMTA Workshop - Specialized Regulatory Pathways
Overview of IMDRF foundational pathways
Devices intended for specific patient populations
Innovative Medical Devices
Regulatory toolboxes to foster innovation