Common specification requirements for in vitro diagnostic devices
MHRA is inviting members of the public, including the patients, medical device researchers, developers, manufacturers and suppliers, clinicians, other healthcare professionals to provide their views on the introduction of common specification requirements to the regulatory framework before IVD devices can be placed on the GB market.
Read the news from Medicines and Healthcare products Regulatory Agency published on 21 May 2024.
OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (5 juillet 2024). Common specification requirements for in vitro diagnostic devices. ELSIBI. Consulté le 10 décembre 2024 à l’adresse https://doi.org/10.58079/11yb6
