首页 >
法规速递
-
Page: Union Product Database-2026/4/9
2026-04-10查看详情 > -
Page: Real-world evidence-2026/5/28
2026-05-29查看详情 > -
Regulatory and procedural guideline: Member states contact points for review of national translations of Quick Response (QR) codes of veterinary medicinal products authorised via the centralised, mutual recognition, decentralised (...)-2023/01/05
2023-01-05查看详情 > -
关于《乙酰半胱氨酸颗粒生物等效性研究指导原则（征求意见稿）》等五项技术指导原则公开征求意见的通知-2023/7/27
2023-07-28查看详情 > -
国家药监局关于修订深海龙丸和深海龙胶囊非处方药说明书范本的公告（2024年第10号）-2024/2/5
2024-03-11查看详情 > -
Page: Product-specific bioequivalence guidance-2025/1/31
2025-02-05查看详情 > -
Document: European Shortages Monitoring Platform (ESMP) data access policy - Annex A: Data elements accessible by ESMP access level-2025/3/10
2025-03-11查看详情 > -
Document: HMPC meeting report on European Union herbal monographs, guidelines and other activities - 17-19 March 2025-2025/4/10
2025-04-11查看详情 > -
Page: ICH M11 guideline, clinical study protocol template and technical specifications - Scientific guideline-2025/5/23
2025-05-26查看详情 > -
关于再次公开征求《多联疫苗临床研究技术指导原则（征求意见稿）》意见的通知-2025/6/30
2025-07-01查看详情 >
