Vancouver, Canada

Meeting no
11
Date
-
Location
Vancouver, Canada

Uncategorized

IMDRF Stakeholder Forum Draft Agenda 15 March 2017
IMDRF Presentation - Stakeholder - AHWP update
IMDRF Presentation - Stakeholder - APEC update - PDF
IMDRF Presentation - Stakeholder - DITTA update
IMDRF Presentation - Stakeholder - GMTA update
IMDRF Presentation - Stakeholder - PAHO update
IMDRF Presentation - Stakeholder - WHO update
IMDRF Presentation - New Work Item Proposal - GMTA

Jurisdictional updates

Australia
Brazil ANVISA
Health Canada
China
EU
Japan
Russia
Singapore
US

Working group updates

Good Regulatory Review Practices
Adverse Event Terminology
Jan 2017
NCAR
Registries
RPS
SaMD Clinical Evaluation
Standards

Member sites

Regional harmonization initiatives

APEC LSIF Regulatory Harmonization Steering Committee

Global Harmonization Working Party (GHWP)

Pan American Health Organization (PAHO)

African Medical Devices Forum (AMDF)

Official observers

Argentina, National Administration of Drugs, Food and Medical Devices

World Health Organization (WHO)

Swissmedic

 

Affiliate members

SAHPRA - South African Health Products Regulatory Authority

TFDA - Taiwan Food and Drug Administration

CECMED (Cuba) - Centro para el Control Estatal de Medicamentos, Equipos y Dispositivos Médicos

EDA - Egyptian Drug Authority 

MTIIR (Israel) - The Medical Technology, Health Information, Innovation and Research Directorate

ISP - Public Health Institute of Chile

CinMED - Institute for Medicine and Medical Devices of Montenegro