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Document: Procedural advice on paediatric applications-2025/7/28
2025-07-29查看详情 > -
国家药监局药审中心关于发布创新药临床试验申请申报资料要求等相关文件的通告（2025年第40号）-2025/9/12
2025-09-12查看详情 > -
Document: Management Board - Outcome of written procedures finalised during the period from 29 June to 22 September 2025-2025/10/16
2025-10-17查看详情 > -
Page: Download website data in JSON data format-2025/11/20
2025-11-21查看详情 > -
Page: Worksharing: questions and answers-2025/12/15
2025-12-16查看详情 > -
Page: ICH Q3E Extractables and leachables - scientific guideline-2026/1/28
2026-01-29查看详情 > -
关于公开征求《治疗用重组蛋白药物上市许可申请质量综述资料撰写指导原则（征求意见稿）》等三个指导原则意见的通知-2026/3/9
2026-03-10查看详情 > -
Page: Data protection and privacy at EMA-2026/4/7
2026-04-08查看详情 > -
关于公开征求《罕见疾病药物开发中疾病自然史研究指导原则》意见的通知-2022/12/21
2022-12-22查看详情 > -
国家药监局综合司公开征求《药品说明书适老化改革试点工作方案》等文件意见-2023/6/29
2023-06-30查看详情 >
