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Registration page
IMDRF Stakeholder Forum Agenda
IMDRF Presentation - Stakeholder - AHWP update
IMDRF Presentation - Stakeholder - APEC update
IMDRF Presentation - Stakeholder - CAMDI update
IMDRF Presentation - Stakeholder - DITTA update
IMDRF Presentation - Stakeholder - GMTA update
IMDRF Presentation - Stakeholder - Hong Kong SAR update
IMDRF Presentation - Stakeholder - Mexico COFEPRIS update
IMDRF Presentation - Stakeholder - PAHO update
IMDRF Presentation - Stakeholder - WHO update
Jurisdictional updates
Australia
Brazil
Canada
China
Japan
Russia
Singapore
South Korea
Working group updates
Adverse Event Terminology
Good Regulatory Review Practices
Medical Device Clinical Evaluation
Personalized Medical Devices
Regulated Products Submission
Standards
Unique Device Identification