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国家药监局关于10批次化妆品检出禁用原料的通告（2025年第16号）-2025/4/27
2025-04-28查看详情 > -
CVM GFI #287 - Raw Data for Safety and Effectiveness Studies-2025/6/4
2025-06-06查看详情 > -
Page: Sharing data across systems: Master data on human medicines-2025/7/10
2025-07-11查看详情 > -
国家药监局关于批准注册295个医疗器械产品的公告(2025年7月)(2025年第77号）-2025/8/20
2025-08-21查看详情 > -
Document: Concept paper on new guidance on the clinical investigation of medicinal products for the treatment of idiopathic pulmonary fibrosis (IPF)-2025/9/30
2025-10-08查看详情 > -
国家药监局关于批准医用电声设备医疗器械标准化技术归口单位换届的公告（2025年第109号）-2025/11/7
2025-11-10查看详情 > -
Document: Applications for new human medicines under evaluation: December 2025-2025/12/5
2025-12-08查看详情 > -
Page: Clinical investigation of medicinal products in the treatment of peripheral-arterial occlusive disease - Scientific guideline-2026/1/15
2026-01-16查看详情 > -
Document: Overview of comments received on Q&A regarding co-processed excipients used in solid oral dosage forms H and V (EMA/CHMP/CVMP/QWP/422493/2024)-2026/2/16
2026-02-26查看详情 > -
《药品现代物流规范化建设指导意见》政策问答-2026/3/25
2026-03-26查看详情 >
