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IMDRF documents

Procedural document

IMDRF/MC/N1FINAL:2023 (Edition 6)

IMDRF Terms of Reference

7 February 2023

Procedural document

IMDRF/MC/N69 FINAL:2023

IMDRF Membership Application Form

7 February 2023

Procedural document

IMDRF/MC/N2 FINAL:2023 (Edition 9)

IMDRF Standard Operating Procedures

6 February 2023

Procedural document

IMDRF/MC/N75 FINAL:2022

IMDRF Working Group Membership Application Form

19 December 2022

Procedural document

IMDRF/MC/N39

IMDRF Strategic Plan 2021-2025

25 September 2020

Procedural document

IMDRF/MC/N16

IMDRF Document Format and Style Guide

23 April 2014

Member sites

Therapeutic Goods Administration

Brazilian Health Regulatory Agency (ANVISA)

Health Canada

National Medical Products Administration

European Commission - Directorate-General for Health and Food Safety

Pharmaceutical and Medical Devices Agency (PMDA)

Russian Ministry of Health

Health Sciences Authority

Ministry of Food and Drug Safety

Medicines and Healthcare products Regulatory Agency

US Food and Drug Administration

Regional harmonization initiatives

APEC LSIF Regulatory Harmonization Steering Committee

Global Harmonization Working Party (GHWP)

Pan American Health Organization (PAHO)

Official observers

Argentina, National Administration of Drugs, Food and Medical Devices

World Health Organization (WHO)

IMDRF documents

Filter by type

IMDRF Terms of Reference

IMDRF Membership Application Form

IMDRF Standard Operating Procedures

IMDRF Working Group Membership Application Form

IMDRF Strategic Plan 2021-2025

IMDRF Document Format and Style Guide

Member sites

Australia

Brazil

Canada

China

European Union

Japan

Russia

Singapore

South Korea

United Kingdom

United States of America

Regional harmonization initiatives

Official observers