Overview Regulation (EU) 2017/745 on Medical Devices (MDR) and Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices (IVDR) are aimed at ensuring… WorkPractical information for expertsExpertsExpert panelsList of opinions provided under the CECPList of views provided and ongoing consultations under the PECPCoordination CommitteeHow to Apply If you are interested to put your expertise at the service of European patients, please consider applying to become a member of an expert panel in… Latest updatesNews announcement27 júl 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)News announcement2 marec 2022Handover of Experts Panels SecretariatNews announcement4 október 2021The EUDAMED UDI/Devices and NBs & Certificates modules are open. Economic Operators and Notified Bodies can start entering data in EUDAMED on voluntary basisNews announcement3 september 2021The expert panel in the field of in vitro diagnostic medical devices now accepts submissions from notified bodies for the Performance Evaluation Consultation ProcedureZobraziť všetky HighlightsCall for expert panels on medical devices and in vitro diagnostic medical devices (2019/C 323/05) Handover of Experts Panels Secretariat DocumentsPublications
News announcement27 júl 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)
News announcement4 október 2021The EUDAMED UDI/Devices and NBs & Certificates modules are open. Economic Operators and Notified Bodies can start entering data in EUDAMED on voluntary basis
News announcement3 september 2021The expert panel in the field of in vitro diagnostic medical devices now accepts submissions from notified bodies for the Performance Evaluation Consultation Procedure
