首页 >
法规速递
-
关于药品审评中心变更临床试验期间药物警戒系统网关电子传输方式提交的通知-2023/11/1
2023-11-07查看详情 > -
Page: Handling competing interests-2025/1/14
2025-01-15查看详情 > -
Document: Checklist for the submission of Type IA and Type IB (without linguistic review) product information annexes and Annex A (if applicable) - human-2025/2/18
2025-02-19查看详情 > -
Document: Guidance for Rapporteurs and members of drafting groups of documents developed by the GMP/GDP Inspectors Working Group-2025/3/27
2025-03-28查看详情 > -
Page: SME Regulation and reports-2025/5/2
2025-05-06查看详情 > -
Document: List of metadata for the HMA-EMA Catalogues of real-world data sources and studies-2025/6/12
2025-06-13查看详情 > -
Page: Paediatric investigation plans: questions and answers-2025/7/17
2025-07-18查看详情 > -
Page: Administration and Corporate Management-2025/9/1
2025-09-02查看详情 > -
Document: Timetable: Companion diagnostic follow-up consultation - ATMP-2025/10/3
2025-10-08查看详情 > -
关于公开征求《中药提取物质量控制研究技术指导原则（征求意见稿）》意见的通知-2025/11/13
2025-11-14查看详情 >
