Work plan for the Committee for Veterinary Medicinal Products (CVMP) Pharmacovigilance Working Party (PhVWP-V) 2025
Work plan for the Committee for Veterinary Medicinal Products (CVMP) Pharmacovigilance Working Party (PhVWP-V) 2025
Work plan for the Committee for Veterinary Medicinal Products (CVMP) Pharmacovigilance Working Party (PhVWP-V) 2025
Policy 44: European Medicines Agency policy on the handling of competing interests of scientific committees’ members and experts - As adopted by EMA Management Board on 11-12 December 2024
Policy 58: European Medicines Agency policy on the handling of competing interests of Management Board members - As adopted by EMA Management Board on 11-12 December 2024
Minutes - HMA-EMA joint Big Data Steering Group teleconference - 11 December 2024
Revised rules on handling of competing interests published
Outcome of Public consultation on Policy 0044 - Summary of comments and EMA feedback
Timetable: Initial (full) marketing authorisation application accelerated assessment timetables
Clinical Trials Information System (CTIS) sponsor end user training programme - November 2025, Online, European Medicines Agency, Amsterdam, the Netherlands, from 25 November 2025, 14:00 (CET) to 28 November 2025, 18:30 (CET)
Timetable: Initial (Full) marketing authorisation application - ATMP
Clinical Trials Information System (CTIS) sponsor end user training programme - March 2025, Online, European Medicines Agency, Amsterdam, the Netherlands, from 25 March 2025, 09:00 (CET) to 28 March 2025, 13:30 (CET)