Consultation closed

Personalized Medical Devices Regulatory Pathways

Start date
Closing date
Working group
Personalized Medical Devices (PMD)

A Proposed Document by the International Medical Device Regulators Forum (IMDRF) Personalized Medical Devices Working Group is provided below for public comment.

Thank you for your contribution in reviewing and providing feedback for this document.

Consultation documents

Personalized Medical Devices Regulatory Pathways

Please use the comments template to provide comments on the Proposed Document and send comments to Personalised Medical Devices team via email: personaliseddevices [at] health.gov.au (personaliseddevices[at]health[dot]gov[dot]au) with the subject line 'Public Consultation on Proposed PMD Regulatory Pathways Working Draft'.

Comments - PMD Regulatory Pathways

Member sites

Regional harmonization initiatives

APEC LSIF Regulatory Harmonization Steering Committee

Global Harmonization Working Party (GHWP)

Pan American Health Organization (PAHO)

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