FDA Issues Guidance to Improve Collection of Pregnancy Safety Data for Drugs and Biologics Par FDA – Press releases
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 4-7 May 2026 Par EMA – News and press releases
Good manufacturing practice: Multistakeholder workshop on expert contributions to artificial intelligence guidance development (Annex 22), Online, European Medicines Agency, Amsterdam, the Netherlands, from 30 June 2026, 09:00 (CEST) to 1 July 2026, 18:00 (CEST) Par EMA – Events
Clinical Trials Information System (CTIS): Information day, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 17 June 2026, 12:30 (CEST) to 17 June 2026, 17:30 (CEST) Par EMA – Events
