首页 >
法规速递
-
Page: Quality of medicines: questions and answers - Part 1-2026/3/2
2026-03-03查看详情 > -
Document: EU implementation strategy of ICH E2D(R1) Guideline - Post-approval safety data: Definitions and standards for management and reporting of individual case safety reports-2026/3/27
2026-03-30查看详情 > -
Document: Applications for new human medicines under evaluation: May 2026-2026/5/11
2026-05-12查看详情 > -
氯雷他定片生物等效性研究技术指导原则-2022/11/25
2022-11-25查看详情 > -
关于公开征求《化学仿制药参比制剂目录（第六十九批）》（征求意见稿）意见的通知-2023/5/4
2023-05-05查看详情 > -
Regulatory and procedural guideline: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure (updated)-2023/11/13
2023-11-15查看详情 > -
Page: Eligible healthcare professionals' organisations-2025/1/16
2025-01-17查看详情 > -
Page: Frequently asked questions-2025/2/20
2025-02-21查看详情 > -
Document: HMPC: overview of assessment work - priority list-2025/3/28
2025-04-01查看详情 > -
Document: UPD registration guide for UI and API users-2025/5/6
2025-05-07查看详情 >
