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Page: Download website data in JSON data format-2026/4/10
2026-04-12查看详情 > -
Scientific guideline: ICH guideline M10 on bioanalytical method validation and study sample analysis – Frequently Asked Questions (FAQ) (updated)-2023/01/13
2023-01-13查看详情 > -
Final Guidance: CDER’s Program for the Recognition of Voluntary Consensus Standards Related to Pharmaceutical Quality-2023/7/26
2023-07-28查看详情 > -
国家药监局关于恢复进口、销售和使用GlaxoSmithKline（Ireland）Limited度他雄胺软胶囊的公告（2024年第15号）-2024/2/8
2024-03-12查看详情 > -
Page: Clinical Trials Information System (CTIS): online training modules-2025/1/31
2025-02-05查看详情 > -
Document: Agenda of the CVMP meeting 11-13 March 2025-2025/3/10
2025-03-11查看详情 > -
Document: CHMP-CAT - D80-210 Overview to final EPAR - Rev 04.25 (Revamp)-2025/4/11
2025-04-13查看详情 > -
Document: Minutes of the Cancer Medicines Forum - March 2025-2025/5/23
2025-05-26查看详情 > -
Page: PRAC recommendations on safety signals-2025/6/30
2025-07-01查看详情 > -
国家药监局综合司公开征求《互联网药品医疗器械信息服务备案管理规定（征求意见稿）》意见 -2025/7/31
2025-08-01查看详情 >
