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 views provided and ongoing consultations under the PECPList of opinions provided under the CECPCoordination 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 announcement23 agosto 2023Ongoing consultations under the PECP - IVD-2023-000017 and IVD-2023-000018News announcement26 luglio 2023Advice on the influenza virus on request from the Medical Device Coordination GroupNews announcement2 marzo 2023Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)News announcement23 gennaio 2023Annual overview of devices subject to the clinical evaluation consultation procedure (CECP) - April 2021- June 2022Mostra tutto 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 views provided and ongoing consultations under the PECPList of opinions provided under the CECPCoordination 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 announcement23 agosto 2023Ongoing consultations under the PECP - IVD-2023-000017 and IVD-2023-000018
News announcement26 luglio 2023Advice on the influenza virus on request from the Medical Device Coordination Group
News announcement2 marzo 2023Expert decision and opinion in the context of the Clinical Evaluation Consultation Procedure (CECP)
News announcement23 gennaio 2023Annual overview of devices subject to the clinical evaluation consultation procedure (CECP) - April 2021- June 2022
