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Document: Minutes – Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) - 17 December 2025-2026/2/2
2026-02-03查看详情 > -
Page: High-risk medical devices: consultation procedures-2026/3/10
2026-03-11查看详情 > -
Page: Establishing maximum residue limits for veterinary medicines-2026/4/8
2026-04-09查看详情 > -
国家药监局关于发布《药品上市许可持有人落实药品质量安全主体责任监督管理规定》的公告（2022年第126号）
2022-12-30查看详情 > -
国家药监局综合司关于同意北京市药品检验研究院增加生物制品批签发证明文件授权签发人的复函-2023/7/17
2023-07-21查看详情 > -
Page: Product-specific bioequivalence guidance-2024/1/15
2024-02-05查看详情 > -
Document: List of industry subject matter experts and list of planned calls for industry subject matter experts-2025/1/29
2025-02-05查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/3/5
2025-03-06查看详情 > -
Document: Minutes of the PRAC meeting 13-16 May 2024-2025/4/9
2025-04-11查看详情 > -
Document: Scientific recommendations on classification of advanced therapy medicinal products-2025/5/21
2025-05-22查看详情 >
