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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

 

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)