首页 >
法规速递
-
Document: Questions and Answers on the Joint Controllership Arrangement and data protection matters related to the use of the Clinical Trials Information System-2026/3/13
2026-03-16查看详情 > -
Document: Procedural advice on paediatric applications-2026/4/16
2026-04-17查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2026/5/29
2026-05-31查看详情 > -
国家药监局药审中心关于发布《慢性淋巴细胞白血病新药临床研发技术指导原则》的通告（2023年第1号）-2023/01/19
2023-01-19查看详情 > -
国家药监局关于修订氯化钾注射剂说明书的公告（2023年第98号）-2023/8/17
2023-08-18查看详情 > -
关于公开征求ICH《Q2（R2）/Q14:分析方法验证和分析方法开发》实施建议和中文版意见的通知-2024/2/18
2024-03-12查看详情 > -
Page: Quality Working Party-2025/2/4
2025-02-05查看详情 > -
Document: Minutes of the PRAC meeting 13-16 January 2025-2025/3/12
2025-03-13查看详情 > -
Page: Contacts at the European Medicines Agency-2025/4/14
2025-04-15查看详情 > -
Page: Quality of medicines questions and answers: Part 1-2025/5/27
2025-05-28查看详情 >
