首页 >
法规速递
-
Stimulant Use Disorders: Developing Drugs for Treatment-2026/5/13
2026-05-15查看详情 > -
Page: Guideline on data requirements for authorisation of immunological veterinary medicinal products in exceptional circumstances - Scientific guideline-2026/6/26
2026-06-29查看详情 > -
Regulatory and procedural guideline: Procedural advice for orphan medicinal product designation: Guidance for sponsors-2022/11/7
2022-11-30查看详情 > -
Scientific guideline: Draft ICH E6 (R3) Guideline on good clinical practice (GCP) - Step 2b-2023/5/26
2023-05-30查看详情 > -
关于公开征求《药品变更受理审查指南（试行）（征求意见稿）》意见的通知-2023/11/28
2023-12-04查看详情 > -
Document: Policy 29: Representing the Agency at external events or in professional bodies-2025/1/20
2025-01-21查看详情 > -
国家药监局综合司关于2025年医疗器械行业标准制修订计划项目公示-2025/2/24
2025-02-25查看详情 > -
Document: Call for scientific data for the periodic review of the monograph on Harpagophyti radix-2025/4/1
2025-04-02查看详情 > -
Page: Opinions and letters of support on the qualification of novel methodologies for medicine development-2025/5/8
2025-05-09查看详情 > -
关于公开征求《创新药临床试验申请申报资料要求》等相关文件（征求意见稿）意见的通知-2025/6/19
2025-06-20查看详情 >
