Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/12/17

Page: Medicine shortages and availability issues: guidance for companies-2025/12/17

Document: Call for user acceptance testers for the read functionality in the Public Product Management Service (PMS) Application Programming Interface (API)-2025/12/17

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

Document: Concept Paper on the revision of Annex 3 of the guidelines on Good Manufacturing Practice for Radiopharmaceuticals-2025/12/17

Document: Overview of (invented) names reviewed in November 2025 by the Name Review Group (NRG) adopted at the CHMP meeting of 11 December 2025-2025/12/17

Document: Agenda - Management Board meeting: 17-18 December 2025-2025/12/17

Document: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group-2025/12/17

Document: QRD Appendix V - Adverse-drug-reaction reporting details-2025/12/17

Document: Name Review Group form - questions and answers-2025/12/17