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Page: Medicines for human use under evaluation-2026/4/1
2026-04-02查看详情 > -
国家药监局关于批准注册318个医疗器械产品的公告（2026年4月）（2026年第46号）-2026/5/18
2026-05-19查看详情 > -
Page: Financial management and budgetary reporting-2026/6/30
2026-07-01查看详情 > -
Page: CHMP opinions on consultation procedures on ancillary substances incorporated in a medical device-2026/8/7
2026-08-09查看详情 > -
国家药监局综合司再次公开征求《中药注册管理专门规定（征求意见稿）》意见-2022/11/11
2022-11-30查看详情 > -
Regulatory and procedural guideline: Guidance on paediatric submissions-2023/6/9
2023-06-12查看详情 > -
国家药监局药审中心关于更新《申报资料电子光盘技术要求》等文件的通知-2023/12/11
2023-12-21查看详情 > -
Document: Appendix 1: Acceptable intakes established for N-nitrosamines-2025/1/22
2025-01-23查看详情 > -
Document: Annex to 24-27 February 2025 CHMP Agenda-2025/2/24
2025-02-25查看详情 > -
Document: Organisation chart: Veterinary Medicines-2025/4/1
2025-04-02查看详情 >
