首页 >
法规速递
-
Document: List of centrally authorised products with safety-related changes to the product information-2026/2/27
2026-02-28查看详情 > -
Document: Info sheet - Orphan medicines in the EU-2026/2/27
2026-02-28查看详情 > -
Document: Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) annual activity report 2025-2026/2/26
2026-02-27查看详情 > -
Document: Minutes of the Management Board meeting: 17-18 December 2025-2026/2/26
2026-02-27查看详情 > -
Document: European Medicines Agency (EMA) stakeholder relations management framework-2026/2/26
2026-02-27查看详情 > -
Document: Standard operating procedure for annual review of VeDDRA list to be used in EudraVigilance Veterinary-2026/2/26
2026-02-27查看详情 > -
Document: New product information wording – Extracts from PRAC recommendations on signals adopted at the 28-31 October 2024 PRAC-2026/2/26
2026-02-27查看详情 > -
Page: Fees payable to the European Medicines Agency: Guidance for all applicants-2026/2/25
2026-02-27查看详情 > -
Page: List of medicines under additional monitoring-2026/2/25
2026-02-27查看详情 > -
Document: List of medicinal products under additional monitoring-2026/2/25
2026-02-27查看详情 >
