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

Document: Agenda - Management Board meeting: 12 March 2026-2026/3/11

Document: List of eligible industry stakeholder organisations-2026/4/9

Document: Timetable: Annual reassessment - ATMP-2026/5/27

Document: Annex to interim measures regarding notification of pharmacovigilance alerts by marketing authorisation holders under Regulation (EU) 2019/6: contact points-2026/7/10