OverviewRegulation (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 ApplyIf 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 announcement20 október 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)News announcement24 august 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)News announcement27 júl 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)News announcement2 marec 2022Handover of Experts Panels SecretariatZobraziť všetky HighlightsCall for expert panels on medical devices and in vitro diagnostic medical devices (2019/C 323/05) Handover of Experts Panels Secretariat DocumentsPublications
OverviewRegulation (EU) 2017/745 on Medical Devices (MDR) and Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices (IVDR) are aimed at ensuring…
ExpertsExpert panelsList of opinions provided under the CECPList of views provided and ongoing consultations under the PECPCoordination Committee
How to ApplyIf 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…
News announcement20 október 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)
News announcement24 august 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)
News announcement27 júl 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)
