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Page: ICH M4Q - The Common Technical Document for the registration of pharmaceuticals for human use - Quality - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Page: Clinical Trials Information System (CTIS): training and support-2026/3/26
2026-03-27查看详情 > -
Document: Minutes of the CAT meeting 18-20 March 2026-2026/5/5
2026-05-06查看详情 > -
Page: Languages on this website-2026/6/16
2026-06-17查看详情 > -
Regulatory and procedural guideline: Guidance on parallel EMA / EUnetHTA 21 Joint Scientific Consultation-2022/10/6
2022-11-15查看详情 > -
国家药监局关于修订白芍总苷胶囊说明书的公告（2023年第48号）-2023/4/24
2023-04-25查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第七十三批）的通告（2023年第54号）-2023/10/26
2023-11-06查看详情 > -
国家药监局关于修订人血白蛋白注射剂说明书的公告（2025年第5号）-2025/1/13
2025-01-14查看详情 > -
Document: Agenda of the COMP meeting 18-19 February 2025-2025/2/17
2025-02-18查看详情 > -
Document: List of medicinal products under additional monitoring-2025/3/26
2025-03-27查看详情 >
