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Page: Classification of changes: questions and answers-2026/1/15
2026-01-16查看详情 > -
Page: ICH E20 adaptive designs for clinical trials - Scientific guideline-2026/2/16
2026-02-26查看详情 > -
国家药监局关于印发药品现代物流规范化建设指导意见的通知-2026/3/25
2026-03-26查看详情 > -
Page: Advisory group on vaccine confidence-2026/4/29
2026-04-30查看详情 > -
关于公开征求ICH《M11：电子结构化协调的临床方案》指导原则及相关文件实施建议和中文翻译稿意见的通知-2026/6/12
2026-06-12查看详情 > -
Facility Readiness: Goal Date Decisions Under GDUFA (Draft)-2022/10/3
2022-11-14查看详情 > -
基于动物法则的药物研究技术指导原则（试行）-2023-4/7
2023-04-10查看详情 > -
关于公开征求《艾曲泊帕乙醇胺片生物等效性研究技术指导原则（征求意见稿）》和《恩扎卢胺软胶囊生物等效性研究技术指导原则（征求意见稿）》意见的通知-2023/10/08
2023-10-08查看详情 > -
Page: Pharmacovigilance Inspectors Working Group-2025/1/7
2025-01-08查看详情 > -
Document: New product information wording – Extracts from PRAC recommendations on signals adopted at the 28-31 October 2024 PRAC-2025/2/13
2025-02-14查看详情 >
