MDCG 21-27 – Questions and Answers on Articles 13 & 14 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746
The document, endorsed by the Medical Device Coordination Group, presents questions and answers on requirements related to importers and distributors under Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR).
Read the news announcement published by the European Commission on 9 December 2021.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (14 mars 2022). MDCG 21-27 – Questions and Answers on Articles 13 & 14 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746. ELSIBI. Consulté le 18 février 2026 à l’adresse https://doi.org/10.58079/o5vg





