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Document: Appendix 1: Acceptable intakes established for N-nitrosamines-2026/3/13
2026-03-16查看详情 > -
Document: List of industry subject matter experts and list of planned calls for industry subject matter experts-2026/4/14
2026-04-15查看详情 > -
关于《化妆品中三价铬和六价铬的检验方法》等8项方法的问答-2026/5/29
2026-05-31查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2026/7/13
2026-07-14查看详情 > -
Scientific guideline: Procedural advice for vaccine platform technology master file (vPTMF) certification-2023/01/27
2023-01-27查看详情 > -
Regulatory and procedural guideline: Questions and answers (Q&As) on the external guidance of Policy 0070 on clinical data publication (CDP) (updated)-2023/8/1
2023-08-02查看详情 > -
国家药监局综合司关于同意江苏省食品药品监督检验研究院 调整生物制品批签发证明文件授权签发人的复函 药监综药管函〔2024〕102号-2024/3/1
2024-03-12查看详情 > -
Page: Cardiovascular Working Party-2025/2/4
2025-02-05查看详情 > -
《国家药监局关于发布医疗器械临床试验项目检查要点及判定原则的公告》政策解读-2025/3/12
2025-03-13查看详情 > -
Document: Questions & answers - Practical arrangements on the companion diagnostics consultation procedure to the European Medicines Agency by notified bodies-2025/4/11
2025-04-13查看详情 >
