3 July 2023 National Requirements for the Local Person for Pharmacovigilance (LPPV) in the EU, UK and Switzerland
22 June 2023 Simplified reporting procedures for monitoring the safety of clinical trials: simplified procedures for sponsors
Q&A Clinic on post-authorisation procedure management in IRIS (2), Online, European Medicines Agency, Amsterdam, the Netherlands, from 19 December 2024, 11:00 (CET) to 19 December 2024, 12:00 (CET) By EMA – Events
European Commission/EMA meeting with stakeholders on Translarna (ataluren), Online, from 10 December 2024, 11:00 (CET) to 10 December 2024, 12:00 (CET) By EMA – Events
Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 3-5 December 2024 By EMA – News and press releases
Q&A Clinic on post-authorisation procedure management in IRIS (1), Online, from 11 December 2024, 11:00 (CET) to 11 December 2024, 12:00 (CET) By EMA – Events
2024 annual meeting of the members and Coordinating Group of the European network of paediatric research at the EMA (Enpr-EMA), Online, European Medicines Agency, Amsterdam, the Netherlands, 1 October 2024 By EMA – Events