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 announcement2 marzec 2023Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)News announcement23 styczeń 2023Annual overview of devices subject to the clinical evaluation consultation procedure (CECP) - April 2021- June 2022News announcement18 styczeń 2023Information session on the pilot for expert panels’ scientific advice to manufacturers of high-risk medical devices - 25 January 2023News announcement20 październik 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)Zobacz wszystko 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 announcement2 marzec 2023Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)
News announcement23 styczeń 2023Annual overview of devices subject to the clinical evaluation consultation procedure (CECP) - April 2021- June 2022
News announcement18 styczeń 2023Information session on the pilot for expert panels’ scientific advice to manufacturers of high-risk medical devices - 25 January 2023
News announcement20 październik 2022Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)
