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 views provided and ongoing consultations under the PECPList of opinions provided under the CECPCoordination 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 announcement | 2 marzo 2022Handover of Experts Panels SecretariatNews announcement | 4 ottobre 2021The EUDAMED UDI/Devices and NBs & Certificates modules are open. Economic Operators and Notified Bodies can start entering data in EUDAMED on voluntary basisNews announcement | 3 settembre 2021The expert panel in the field of in vitro diagnostic medical devices now accepts submissions from notified bodies for the Performance Evaluation Consultation ProcedureNews announcement | 1 aprile 2021The expert panels in the field of medical devices now accept submissions from notified bodies for the Clinical Evaluation Consultation ProcedureMostra tutto HighlightsCall for expert panels on medical devices and in vitro diagnostic medical devices (2019/C 323/05) Handover of Experts Panels Secretariat DocumentsPublications
News announcement | 4 ottobre 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 announcement | 3 settembre 2021The expert panel in the field of in vitro diagnostic medical devices now accepts submissions from notified bodies for the Performance Evaluation Consultation Procedure
News announcement | 1 aprile 2021The expert panels in the field of medical devices now accept submissions from notified bodies for the Clinical Evaluation Consultation Procedure
