首页 >
法规速递
-
Page: ICH E2D post-approval safety data management - scientific guideline-2025/11/17
2025-11-18查看详情 > -
Document: Work plan for the European Sales and Use of Antimicrobials in veterinary medicine Working Group (ESUAvet WG) 2026-2025/12/12
2025-12-15查看详情 > -
Page: Medical device expert panels-2026/1/26
2026-01-27查看详情 > -
Document: Darwin EU study: Overall survival in patients with non-small cell lung cancer treated with selected immunotherapies-2026/3/4
2026-03-05查看详情 > -
Document: Implantable cardiac devices (various) - Notified body 2797 - 15/07/2025 - Expert decision and opinion in the context of the clinical evaluation consultation procedure (CECP)-2026/4/1
2026-04-02查看详情 > -
Regulatory and procedural guideline: IRIS guide to registration and RPIs-2022/11/21
2022-11-30查看详情 > -
关于公开征求《化学仿制药参比制剂目录（第七十批）》（征求意见稿）意见的通知-2023/6/1
2023-06-02查看详情 > -
国家药监局药审中心关于发布《药品说明书（简化版）及药品说明书（大字版）编写指南》和《电子药品说明书（完整版）格式要求》的通告（2023年第56号）-2023/11/28
2023-12-21查看详情 > -
Document: Agenda of the COMP meeting 21-23 January 2025-2025/1/21
2025-01-22查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2025/2/24
2025-02-25查看详情 >
