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Page: Recommendations on medication errors-2026/4/16
2026-04-17查看详情 > -
医疗器械分类调整相关公告解读-2026/6/1
2026-06-02查看详情 > -
Formal Meetings Between the Food and Drug Administration and Sponsors or Requestors of Over-the-Counter Monograph Drugs-2026/7/14
2026-07-15查看详情 > -
Considerations for the Design and Conduct of Externally Controlled Trials for Drug and Biological Products(Draft)-2023/01/31
2023-01-31查看详情 > -
国家药监局综合司公开征求《药品附条件批准上市申请审评审批工作程序（试行） （修订稿征求意见稿）》意见-2023/8/25
2023-08-25查看详情 > -
国家药监局药审中心关于发布《小儿便秘中药新药临床研发技术指导原则（试行）》的通告（2024年第19号）-2024/3/1
2024-03-12查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/2/5
2025-02-06查看详情 > -
Document: CTIS newsflash - 11 March 2025-2025/3/12
2025-03-13查看详情 > -
Page: Product-information (QRD) templates - Human-2025/4/14
2025-04-15查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/5/28
2025-05-29查看详情 >
