Consultation closed

Competence, Training and Conduct Requirements for Regulatory Reviewers

Start date
Closing date
Working group
Good Regulatory Review Practices

A proposed document has been released by the International Medical Device Regulators Forum (IMDRF) Good Regulatory Review Practices Working Group.

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

Consultation documents

Competence, Training, and Conduct Requirements for Regulatory Reviewers

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