EMA establish advisory portal for high-risk medical devices
The European Medicines Agency (EMA), in collaboration with the European Commission (EC), has established a standard procedure for manufacturers of certain high-risk medical devices to request scientific advice on their planned clinical development strategy and proposals for clinical investigation. The post EMA establish advisory portal for high-risk medical devices appeared first on Medical Device Network.
The European Medicines Agency (EMA), in collaboration with the European Commission (EC), has established a standard procedure for manufacturers of certain high-risk medical devices to request scientific advice on their planned clinical development strategy and proposals for clinical investigation.
The post EMA establish advisory portal for high-risk medical devices appeared first on Medical Device Network.
