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国家药监局关于发布互联网药品医疗器械信息服务备案管理规定的公告（2025年第123号）-2025/12/22
2025-12-23查看详情 > -
Document: European Medicines Agency’s data protection notice for EudraVigilance Human (EV)-2026/2/5
2026-02-06查看详情 > -
Page: Union Product Database-2026/3/13
2026-03-16查看详情 > -
Document: Article 57 product data-2026/4/14
2026-04-15查看详情 > -
国家药监局关于将《化妆品中三价铬和六价铬的检验方法》等8项方法纳入化妆品安全技术规范的公告（2026年第51号） -2026/5/29
2026-05-31查看详情 > -
Document: Template - Application for transfer of marketing authorisation from transferor to transferee, attachment 1-2026/7/13
2026-07-14查看详情 > -
Regulatory and procedural guideline: Guideline on the application of Article 34 of Regulation (EU) 2019/6-2023/01/27
2023-01-27查看详情 > -
Regulatory and procedural guideline: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure (updated)-2023/7/31
2023-08-02查看详情 > -
国家药监局综合司关于同意广东省药品检验所调整生物制品批签发证明文件授权签字人的复函 药监综药管函〔2024〕91号-2024/3/1
2024-03-12查看详情 > -
Page: Availability of medicines before and during crises-2025/2/3
2025-02-05查看详情 >
