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Document: New product information wording: extracts from PRAC recommendations on signals adopted at the 27-30 October 2025 PRAC-2025/11/24
2025-11-25查看详情 > -
Page: European Shortages Monitoring Platform (ESMP): Interoperability with national and pharmaceutical industry systems-2025/12/16
2025-12-17查看详情 > -
Document: Concept paper on the revision of the guideline on clinical evaluation of diagnostic agents and its appendix 1 on imaging agents-2026/1/30
2026-02-02查看详情 > -
国家药监局关于注销胚胎培养箱等9个医疗器械注册证书的公告(2026年第23号)-2026/3/10
2026-03-11查看详情 > -
Document: Veterinary medicine safety day: How to dispose of unused veterinary medicines-2026/4/8
2026-04-09查看详情 > -
国家药监局药审中心关于将补充资料通知由纸质邮寄调整为电子推送有关事宜的通知-2022/12/28
2022-12-29查看详情 > -
Regulatory and procedural guideline: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2023/7/5
2023-07-07查看详情 > -
国家药监局关于发布仿制药参比制剂目录(第七十六批)的通告(2024年第8号)-2024/2/4
2024-02-05查看详情 > -
Document: European Shortages Monitoring Platform (ESMP): Implementation guide for marketing authorisation holders-2025/1/29
2025-02-05查看详情 > -
Page: Medicines for human use under evaluation-2025/3/4
2025-03-05查看详情 >