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Regulated Product Submission - Assembly and Technical Guide for IMDRF Table of Contents (ToC) Submissions

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Regulated Product Submission

A proposed document was released by the International Medical Device Regulators Forum (IMDRF) Regulated Product Submission Table of Contents Working Group.

Thank you for your contribution aiming at the validation of this IMDRF Guidance document.

Consultation documents

RPS: Assembly and Technical Guide for IMDRF Table of Contents (ToC) Submissions

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