Freyr provides Swiss Authorized Representative (CH-REP) services to foreign medical device manufacturers for product registration and market entry in the Switzerland.
We act as a Swiss Authorized Representative (CH-REP) to the Swiss Authorities for Medical Devices Manufacturers located outside Switzerland
The European Commission provides a range of guidance documents to assist stakeholders in implementing the medical devices regulations. Legally non-binding... –The European Medical Device Nomenclature (EMDN) – the nomenclature of use in EUDAMED! The European Medical Device Nomenclature (EMDN) will be...
(R) manufacturer, in conjunction with the appropriate VHA Account Manager, will communicate a request for tier revision or hospital exception level pricing to the VHA Medical/Surgical Business Unit ("MSBU") Product Management on a VHA PLUS(R) HOSPITAL EXCEPTION LEVEL PRICING (HELP) form (...