Washington D.C, USA
Jurisdictional updates
Australian jurisdictional update
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IMDRF Presentation - Update on the Brazilian regulatory aspects on medical devices
IMDRF Presentation - Regulatory and Policy Updates - Therapeutic Products Directorate - Health Canada
IMDRF Presentation - Update on EU regulatory developments
IMDRF Presentation - New Direction of Japanese Regulations on MD/IVD - Japan Update
IMDRF Presentation - U.S. FDA Center for Devices and Radiological Health update
IMDRF Presentation - RPS Work Item: Beta Testing of Message Standard
IMDRF Presentation - New Work Item Proposal - Harmonization of Good Clinical Practices
IMDRF Presentation - Medical Device Single Audit Program (MDSAP) Working Group
IMDRF Presentation - Software as a Medical Device (SaMD): Possible Framework for Risk Categorization and Corresponding Considerations - Proposed Final
IMDRF Presentation - Development of common terminology and code related to adverse event of medical device
IMDRF Presentation - RPS Work Item: Table of Contents