San Fransisco, CA, USA

Meeting no
5
Date
-
Location
San Fransisco, CA, USA

Uncategorized

IMDRF Presentation - Final Report Phase One: "List of international standards recognized by IMDRF management committee members"
IMDRF Presentation - Regulatory update: Europe
IMDRF Presentation - Regulatory update: Australia
IMDRF Presentation - Regulatory update: Brazil
IMDRF Presentation - Regulatory update: Canada
IMDRF Presentation - Regulatory update: Japan
IMDRF Presentation - Regulatory update: United States of America
IMDRF Presentation - RPS Work Item: Beta Testing of Message Standard
IMDRF Presentation - Medical Device Single Audit Program (MDSAP) Working Group
IMDRF Presentation - IMDRF Work Item National Competent Authority Report Exchange Criteria and Report Form
IMDRF Presentation - Software as a Medical Device (SaMD)
IMDRF Presentation - RPS Work Item: International Harmonized Structures (formerly Table of Contents)
IMDRF Annual report 2013

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

 

Chile - Public Health Institute of Chile (ISP)

Chinese Taipei Taiwan Food and Drug Administration (TFDA)

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

Egypt - Egyptian Drug Authority  (EDA)

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

Montenegro - Institute for Medicine and Medical Devices of Montenegro (CINMED)

Nigeria - National Agency for Food and Drug Administration Control (NAFDAC)

South Africa - South African Health Products Regulatory Authority (SAHPRA)