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Document: Standard operating procedure for validation, publication, and maintenance of real-world data sources and studies in the HMA-EMA RWD Catalogues-2025/5/19
2025-05-20查看详情 > -
Unique Device Identifier Requirements for Combination Products-2025/6/25
2025-06-27查看详情 > -
Page: Sitagliptin product-specific bioequivalence guidance-2025/7/30
2025-07-31查看详情 > -
Page: Mpox-2025/9/16
2025-09-17查看详情 > -
Page: Development of new medicinal products for the treatment of ulcerative colitis - Scientific guideline-2025/10/22
2025-10-23查看详情 > -
关于公开征求《“三结合”中药注册审评证据体系下临床试验的一般原则（征求意见稿）》意见的通知-2025/11/25
2025-11-26查看详情 > -
国家药监局关于撤销外周可调弯导引导管医疗器械注册证的公告（2025年第122号）-2025/12/17
2025-12-18查看详情 > -
Document: Organisation chart: Human Medicines-2026/2/2
2026-02-03查看详情 > -
Page: Portfolio and technology meetings-2026/3/10
2026-03-11查看详情 > -
Document: Veterinary medicine safety day 2026: Image carousel-2026/4/8
2026-04-09查看详情 >
