The draft document on Good Reliance Practices in regulatory decision-making for medical products: high level principles and considerations is under public consultation.

Please send your comments to Marie Valentin (valentinm@who.int) and Carolyn Doucelin (doucelinc@who.int) no later than 18 September 2020.

Further information:

https://www.who.int/medicines/areas/quality_safety/quality_assurance/projects/en/

https://www.who.int/medicines/areas/quality_safety/quality_assurance/QAS20_851_Rev_1_Good_Reliance_Practices.pdf?ua=1