In vitro diagnostic medical devices: guidance on legislation
Guidance explaining the main features of the Medical Devices Regulations 2002 (SI 2002 No 618, as amended) in relation to in vitro diagnostic medical devices.
Read the press release from Medicines and Healthcare products Regulatory Agency published on 17 July 2023.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (4 septembre 2023). In vitro diagnostic medical devices: guidance on legislation. ELSIBI. Consulté le 19 janvier 2025 à l’adresse https://doi.org/10.58079/o6d7
