EMA – Medical devices: new guidance for industry and notified bodies
A new revision of the guidance available to applicants, marketing authorisation holders and notified bodies of medical devices has been published today. This question-and-answer document provides practical considerations on the implementation of the medical devices and in vitro diagnostic regulations for combinations of medicinal products and medical devices.
More information on the EMA Website.
OpenEdition vous propose de citer ce billet de la manière suivante :
vroby (4 octobre 2024). EMA – Medical devices: new guidance for industry and notified bodies. ELSIBI. Consulté le 10 décembre 2024 à l’adresse https://doi.org/10.58079/12f8x
