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Document: Product Management Service (PMS) roadmap-2025/1/24
2025-02-05查看详情 > -
Document: Minutes of the CAT meeting 22-24 January 2025-2025/2/27
2025-03-03查看详情 > -
国家药监局关于进一步做好《药品生产许可证》发放有关事项的公告政策解读-2025/4/7
2025-04-08查看详情 > -
Document: External guidance on the implementation of the European Medicines Agency policy on the publication of clinical data for medicinal products for human use - Version 1.5-2025/5/15
2025-05-16查看详情 > -
国家药监局关于发布YY 0300—2025《牙科学 修复用人工牙》等38项医疗器械行业标准的公告（2025年第59号）-2025/6/25
2025-06-26查看详情 > -
Document: Response to Paediatric Committee request for supplementary information and modification of proposed PIP (RSI) - Re-submission following clock-stop-2025/7/28
2025-07-29查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第九十六批）的通告（2025年第34号） -2025/9/12
2025-09-12查看详情 > -
Document: Minutes of the CVMP meeting 10-12 June 2025-2025/10/16
2025-10-17查看详情 > -
《药品生产企业出口药品检查和出口证明管理规定》政策解读-2025/11/21
2025-11-24查看详情 > -
Investigator Responsibilities – Safety Reporting for Investigational Drugs and Devices-2025/12/15
2025-12-16查看详情 >
