Avec COETIC, optimisez votre conformité réglementaire

Audit, Formation et Accompagnement de vos projets réglementés

mercredi 30 octobre 2019

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

21 October 2019 Rev.1
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.