Document: Minutes of the CHMP meeting on 14-17 October 2024-2025/3/7

Document: List of medicines currently in PRIME scheme-2025/4/9

Document: Orientation guide for delegates - EMA building-2025/5/22

Document: List of changes to combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animal and humans to veterinary medicinal products for 2024-2025/6/27

Document: List of medicinal products under additional monitoring-2025/7/30

Document: Questions and answers on Implementing Regulation (EU) 2025/1466: Amendment of Regulation (EU) No 520/2012 and Conclusion of the Signal Detection in EudraVigilance Pilot by marketing authorisation holders-2025/9/17

Document: Clinical Trial Information System (CTIS) structured data form - Notifications, Annual Safety Report (ASR) and results-2025/10/23

Document: Expected publication dates of PRAC recommendations on safety signals-2025/11/26

Document: Shortage Prevention Plan (SPP) and Shortage Mitigation Plan (SMP) pilot report-2025/12/17

Cybersecurity in Medical Devices: Quality Management System Considerations and Content of Premarket Submissions-2026/2/3