In vitro diagnostics and the European Database on Medical Devices (EUDAMED) - guide — EUbusiness.com

The European Commission proposed on 23 January more time for companies to apply the In Vitro Diagnostic Medical Devices Regulation (IVDR), under certain conditions, as well as measures to enhance transparency in the medical device sector including speeding up the launch of some elements of the European Database on Medical Devices - EUDAMED.

Related Keywords

,European Union ,European Commission ,Device Coordination Group ,European Database ,Medical Devices ,Vitro Diagnostic Medical Devices Regulation ,Diagnostic Medical ,Vitro Diagnostic Medical Device Regulation ,Medical Devices Regulation ,Member States ,Medical Device Coordination Group ,Member State ,Medical Device Regulation ,Health ,