首页 >
法规速递
-
Page: Archive of development of good pharmacovigilance practices-2026/2/6
2026-02-09查看详情 > -
Document: Records of data processing activity for women leadership development and mentoring activities-2026/3/17
2026-03-18查看详情 > -
国家药监局综合司公开征求《药品经营质量管理规范附录:药品零售连锁质量管理(征求意见稿)》意见-2026/4/20
2026-04-21查看详情 > -
Document: Data protection notice for legal entity and bank account validation regarding payments-2026/6/2
2026-06-02查看详情 > -
Document: PRIME eligibility requests: 2027 deadlines for submission and timetable for assessment-2026/7/14
2026-07-15查看详情 > -
Regulatory and procedural guideline: Validation checklist for Type II quality variations (updated)-2023/02/10
2023-02-10查看详情 > -
关于公开征求《化学仿制药参比制剂目录(第七十三批)》(征求意见稿)意见的通知-2023/8/30
2023-09-01查看详情 > -
国家药监局药审中心关于发布《化学药品注册受理审查指南(试行)》的通告(2025年第14号)-2025/2/9
2025-02-10查看详情 > -
Document: Drug-Eluting stent (DES) - Notified Body 2265 - 10/01/2025 - Expert decision and opinion in the context of the clinical evaluation consultation procedure (CECP)-2025/3/13
2025-03-14查看详情 > -
Document: Policy 26: Records management and archives policy-2025/4/15
2025-04-16查看详情 >