Q&A on the interface between Regulation (EU) 536/2014 on clinical trials for medicinal products for human use (CTR) and Regulation (EU) 2017/746
This Q&A intends to clarify certain interfaces between the Regulation (EU) No 536/2014 on clinical trials for medicinal products for human use (CTR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR)1.
Read the news announcement published by Directorate-General for Health and Food Safety on 25 May 2022.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (20 juillet 2022). Q&A on the interface between Regulation (EU) 536/2014 on clinical trials for medicinal products for human use (CTR) and Regulation (EU) 2017/746. ELSIBI. Consulté le 17 février 2026 à l’adresse https://doi.org/10.58079/o5zs





