18 janvier 2023 La Commission Européenne propose une extension de la période transitoire pour la re-certification des dispositifs médicaux.
22 novembre 2021 Points clés du nouveau règlement européen sur les dispositifs médicaux (UE) 2017/745.
Paediatric Oncology Strategy Forum: 24-25 October 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 24 October 2024 to 25 October 2024 Par EMA – Events
Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 16-18 April 2024 Par EMA – News and press releases
Industry Update webinar on Regulatory Procedure Management for Product Lifecycle Management on IRI, Online, European Medicines Agency, Amsterdam, the Netherlands, from 13 June 2024, 10:00 (CEST) to 13 June 2024, 11:30 (CEST) Par EMA – Events
Network Update webinar on Regulatory Procedure Management for Product Lifecycle Management on IRIS, Online, European Medicines Agency, Amsterdam, the Netherlands, from 18 June 2024, 10:00 (CEST) to 18 June 2024, 11:30 (CEST) Par EMA – Events
Product Management Service (PMS) Product UI and API training (access & navigation), Online, European Medicines Agency, Amsterdam, the Netherlands, from 3 June 2024, 10:00 (CEST) to 3 June 2024, 11:30 (CEST) Par EMA – Events