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Safety Labeling Changes—Implementation of Section 505(o)(4) of the FD&C Act-2025/9/18
2025-09-19查看详情 > -
Page: Ethical use of animals in medicine testing-2025/10/24
2025-10-27查看详情 > -
Document: List of medicinal products under additional monitoring-2025/11/26
2025-11-27查看详情 > -
Questions and Answers Regarding Mandatory Cosmetics Recalls: Guidance for Industry-2025/12/17
2025-12-19查看详情 > -
Document: Hearing the Association of the European Self-Medication Industry (AESGP) during the HMPC November 2025 meeting-2026/2/4
2026-02-05查看详情 > -
国家药监局 国家卫生健康委 国家医保局关于做好后续品种实施医疗器械唯一标识工作的公告（2026年第21号）-2026/3/13
2026-03-16查看详情 > -
Page: Download medicine data-2026/4/10
2026-04-12查看详情 > -
ICH M10 on bioanalytical method validation - Scientific guideline (updated)-2023/01/13
2023-01-13查看详情 > -
Regulatory and procedural guideline: Guidance document on voting in the framework of discussion and adoption of CHMP opinions-2023/7/26
2023-07-28查看详情 > -
国家药监局关于修订裸花紫珠制剂说明书的公告（2024年第17号）-2024/2/23
2024-03-12查看详情 >
