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国家药监局关于修订金乌骨通胶囊药品说明书的公告（2023年第47号）-2023/4/24
2023-04-25查看详情 > -
国家药监局综合司关于印发药品上市许可持有人委托生产现场检查指南的通知-2023/10/24
2023-11-06查看详情 > -
国家药监局综合司关于《采用脑机接口技术的医疗器械 用于人工智能算法的脑电数据集质量要求与评价方法》推荐性医疗器械行业标准立项的公示-2025/1/13
2025-01-14查看详情 > -
Document: New product information wording – Extracts from PRAC recommendations on signals adopted at the 28-31 October 2024 PRAC-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 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/4/30
2025-05-06查看详情 > -
Document: Quality control of medicinal product data submitted as per the legal requirement introduced by Article 57(2) of Regulation (EC) No. 726/2004-2025/6/10
2025-06-11查看详情 > -
Page: Changing the labelling and package leaflet (Article 61(3) notifications)-2025/7/15
2025-07-16查看详情 > -
关于公开征求ICH《E6（R3）：药物临床试验质量管理规范技术指导原则（GCP）》原则及附件1实施建议意见的通知-2025/8/28
2025-08-29查看详情 > -
Page: Fees for human medicines-2025/10/2
2025-10-08查看详情 >
