Berlin, Germany (hosted by European Commission on behalf of the EU)

Meeting no

Jurisdictional Updates

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

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