Kyoto, Japan

Meeting no
8
Date
-
Location
Kyoto, Japan

Working group updates

Adverse Event Terminology and Coding Working Group update
MDSAP Working Group update
RPS Working Group update
SaMD Working Group update

Uncategorized

IMDRF Presentation - AHWP Activity update
IMDRF Presentation - DITTA contribution to stakeholder forum
IMDRF Presentation - NCAR update
IMDRF Presentation - QA session
IMDRF Presentation - RPS - Table of Contents update
IMDRF Presentation - SaMD Survey Results update
IMDRF Presentation - WHO update
IMDRF Presentation - NCAR Implementation update
IMDRF Presentation - GMTA update
IMDRF Presentation - RPS Panel discussion
IMDRF Presentation - PAHO update
IMDRF Presentation - APEC LSIF RHSC update
IMDRF Presentation - Device Registries update - PDF
IMDRF Presentation - NCAR Workshop NMA update

Jurisdictional updates

Brazil
Canada
Japan
US
EU
Australia
Russia
China

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)