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Document: Draft guidance on the conduct of clinical trials during public health emergencies-2026/3/4
2026-03-05查看详情 > -
Document: Records of data processing activity for the Union Product Database-2026/4/1
2026-04-02查看详情 > -
国家药监局关于医用透明质酸钠产品管理类别的公告(2022年第103号)-2022/11/14
2022-11-30查看详情 > -
国家药监局关于银黄含化滴丸和热炎宁合剂转换为非处方药的公告(2023年第75号)-2023/6/20
2023-06-21查看详情 > -
Draft Guidance: Interim Policy on Compounding Using Bulk Drug Substances Under Section 503A of the Federal Food, Drug, and Cosmetic Act-2023/12/6
2023-12-21查看详情 > -
Document: Dates of 2025 Scientific Advice Working Party (SAWP) meetings and submission deadlines for scientific advice, protocol assistance, qualification of novel methodologies and HTACG/EMA parallel Joint Scientific Consultation (JSC) requests-2025/1/22
2025-01-23查看详情 > -
Document: List of medicinal products under additional monitoring-2025/2/24
2025-02-25查看详情 > -
Document: Biologics Working Party Vaccines Quality Operational Expert Group (BV-OEG) Influenza Meeting: EU recommendations for the seasonal influenza vaccine composition for the season 2025/2026-2025/4/1
2025-04-02查看详情 > -
Document: European Shortages Monitoring Platform (ESMP): National competent authority reporting templates-2025/5/13
2025-05-14查看详情 > -
Document: Outcome of written procedures finalised during the period from 4 March 2025 to 28 May 2025-2025/6/19
2025-06-20查看详情 >