首页 >
法规速递
-
Regulatory and procedural guideline: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure-2022/11/4
2022-11-30查看详情 > -
Final Guidance: Adjusting for Covariates in Randomized Clinical Trials for Drugs and Biological Products-2023/5/25
2023-05-30查看详情 > -
关于公开征求《罕见疾病药物临床研发中应用去中心化临床试验的技术指导原则》意见的通知-2023/11/24
2023-11-28查看详情 > -
Document: Agenda: SPOR & XEVMPD status update webinar - 22 January 2025-2025/1/20
2025-01-21查看详情 > -
Page: Infectious Diseases Working Party-2025/2/21
2025-02-24查看详情 > -
Document: Call for scientific data for the periodic review of the monograph on Hamamelidis folium-2025/4/1
2025-04-02查看详情 > -
Page: Supporting innovation-2025/5/8
2025-05-09查看详情 > -
Document: Concept paper on the new reflection paper on the clinical investigation of medicinal products for the treatment of systemic sclerosis-2025/6/18
2025-06-19查看详情 > -
Document: Anti-t lymphocyte immunoglobulin for human use, rabbit : List of nationally authorised medicinal products - PSUSA/00010252/202406-2025/7/23
2025-07-24查看详情 > -
国家药监局综合司公开征求《处方药网络零售合规指南（征求意见稿）》意见-2025/9/8
2025-09-09查看详情 >
