首页 >
法规速递
-
国家药监局综合司关于启用新版《药品生产许可证》《放射性药品生产许可证》样式的通知-2025/10/30
2025-10-31查看详情 > -
Current Good Manufacturing Practice for Medical Gases-2025/11/28
2025-12-01查看详情 > -
国家药监局关于修订活力苏口服液说明书的公告（2025年第131号） -2025/12/31
2026-01-03查看详情 > -
Document: Comments received from public consultation on good pharmacovigilance practices (GVP) Product- or Population-Specific Considerations III: Pregnant and breastfeeding women (EMA/653036/2019)-2026/2/6
2026-02-09查看详情 > -
Document: Agenda - Medicine Shortages SPOC Working Party meeting 16-17 March 2026-2026/3/17
2026-03-18查看详情 > -
Document: Validation checklist for initial marketing authorisation applications - biologicals other than immunologicals (applicable to submissions under Regulation (EU) 2019/6)-2026/4/20
2026-04-21查看详情 > -
Page: Website outages and upgrades-2026/6/2
2026-06-03查看详情 > -
Regulatory and procedural guideline: Questions & Answers regarding Cannabis-derived medicinal products and the scope of EU herbal monographs for herbal medicinal products within the EU medicines legislation-2023/02/15
2023-02-15查看详情 > -
Final Guidance: Considerations for the Use of Real-World Data and Real-World Evidence To Support Regulatory Decision-Making for Drug and Biological Products-2023/8/30
2023-09-01查看详情 > -
国家药监局关于注销空气压力治疗仪等3个医疗器械注册证书的公告（2024年第154号）-2025/1/2
2025-01-03查看详情 >
