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国家药监局 海关总署关于药用类麻醉药品和精神药品进出口申报事项的公告（2025年第110号）-2025/11/14
2025-11-17查看详情 > -
Page: Union Product Database-2025/12/10
2025-12-11查看详情 > -
关于公开征求ICH《E22：患者偏好研究的一般考虑》指导原则草案意见的通知-2026/1/23
2026-01-26查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2026/2/27
2026-02-28查看详情 > -
Document: Data Quality Framework for EU medicines regulation: application to Real-World Data-2026/3/27
2026-03-30查看详情 > -
关于公开征求《间充质干细胞产品药学研究与评价技术指导原则（征求意见稿）》意见的通知-2026/5/11
2026-05-12查看详情 > -
国家药监局药审中心关于发布《富马酸丙酚替诺福韦片生物等效性研究技术指导原则》的通告（2022年第42号）-2022/11/25
2022-11-25查看详情 > -
Scientific guideline: Concept paper on revision of the Guideline on clinical investigation of medicinal products in the treatment of patients with acute respiratory distress syndrome-2023/5/4
2023-05-05查看详情 > -
Final Guidance: Submitting Patient-Reported Outcome Data in Cancer Clinical Trials-2023/11/3
2023-11-07查看详情 > -
Document: Information on the Member States requirement for the nomination of a pharmacovigilance (PhV) contact person at national level-2025/1/15
2025-01-16查看详情 >
