Shanghai, China

Meeting no
13
Date
-
Location
Shanghai, China

Uncategorized

Registration form
DITTA Workshop Registration
DITTA Workshop Presentations
China Stakeholder Forum Agenda - Wednesday 21 March 2018
IMDRF Presentation - Stakeholder - CAMDI update
IMDRF Presentation - Stakeholder - DITTA update
IMDRF Presentation - Stakeholder - GMTA update
IMDRF Presentation - Stakeholder - PAHO update
IMDRF Presentation - Stakeholder - Saudi Arabia update
IMDRF Presentation - Stakeholder - WHO update

Jurisdictional updates

Australia
ANVISA
Canada
China
EU
Japan
Russia
Singapore
South Korea
US

Working group updates

Adverse Event Terminology
Good Regulatory Review Practices
Patient Registry
Personalized Medical Devices
Regulated Products Submission
Standards
Unique Device Identification

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