EMA: Updated and revised Q&A on MDR and IVDR



21 October 2019 Rev.1
EMA/37991/2019
Human Medicines Evaluation Division
Questions & Answers on Implementation of the Medical
Devices and In Vitro Diagnostic Medical Devices Regulations ((EU) 2017/745 and (EU) 2017/746)
This Question and Answer (Q&A) document provides practical considerations concerning the implementation of the medical devices and the in vitro diagnostic medical devices regulations.

Plus d'information ici.

Posts les plus consultés de ce blog

On déménage...

USA : un site destiné à gérer la distribution des vaccins contre la Covid-19 de 44 millions $ construit par Deloitte abandonné à cause des bogues informatiques