首页 >
法规速递
-
Page: Epidemiological data on blood transmissible infections - Scientific guideline-2026/2/4
2026-02-05查看详情 > -
Document: Concept paper on the development of a reflection paper on proof-of-concept data to support the development of anti-cancer medicinal products in paediatric patients-2026/3/13
2026-03-16查看详情 > -
国家药监局药审中心关于发布《以患者为中心的中药新药临床研发技术指导原则》的通告(2026年第29号)-2026/4/13
2026-04-14查看详情 > -
Document: European Medicines Agency’s privacy statement for legal entity and bank account validation-2026/5/28
2026-05-29查看详情 > -
Page: Type-II variations: questions and answers-2026/7/13
2026-07-14查看详情 > -
Document: Timetable: Post-authorisation measure (PAM) assessed by CAT-2026/8/18
2026-08-19查看详情 > -
Regulatory and procedural guideline: Information note on the format and validity features of electronic certificates for medicines issued by the European Medicines Agency (updated)-2023/01/16
2023-01-16查看详情 > -
关于公开征求《基于药代动力学方法支持用于肿瘤治疗的抗PD-1/PD-L1抗体可替换给药方案的技术指导原则(征求意见稿)》意见的通知-2023/8/1
2023-08-02查看详情 > -
国家药监局综合司关于印发药品网络交易第三方平台检查指南(试行)的通知 药监综药管函〔2023〕691号-2024/1/5
2024-03-12查看详情 > -
Page: Guidance on good manufacturing practice and good distribution practice: Questions and answers-2025/1/31
2025-02-05查看详情 >