Web Conference (hosted by Singapore)

Meeting no
18
Date
-
Location
Singapore

Presentations from IMDRF-DITTA Joint Virtual Workshop (21 September)

General updates

IMDRF Stakeholder Forum Programme (23 September)

Jurisdictional updates

Australia
Brazil
Canada
China
EU
Japan
Russia
Singapore
South Korea
US

Working group updates

Regulated Product Submission
Good Regulatory Review Practice
Medical Device Adverse Event Terminology
Personalized Medical Devices
Medical Device Clinical Evaluation
Medical Device Cybersecurity Guide
Principles of In Vitro Diagnostic (IVD) Medical Devices Classification
Artificial Intelligence Medical Devices

Stakeholders updates

IMDRF Presentation - Stakeholder Update - WHO
IMDRF Presentation - Stakeholder Update - APEC LSIF RHSC
IMDRF Presentation - Stakeholder Update - AHWP
IMDRF Presentation - Stakeholder Update - PAHO
IMDRF Presentation - Stakeholder Update - DITTA
IMDRF Presentation - Stakeholder Update - GMTA
IMDRF Presentation - Stakeholder Update - SMF-MTIG
IMDRF Presentation - Stakeholder Update - APACMed

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)