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图解海报 |《医疗器械网络销售质量管理规范》系列解读（三）-2025/6/13
2025-06-16查看详情 > -
Document: Timetable: Annual renewal application of conditional marketing authorisation-2025/7/17
2025-07-18查看详情 > -
Page: World Health Organization (WHO)-2025/9/1
2025-09-02查看详情 > -
Document: Scientific advice on MRL classification of chemical-unlike biological substances considered as not requiring an MRL evaluation according to Regulation (EU) 2018/782-2025/10/6
2025-10-08查看详情 > -
Document: Draft guideline on non-inferiority and equivalence comparisons in clinical trials-2025/11/13
2025-11-14查看详情 > -
2025年12月10日中药品种保护受理公示-2025/12/10
2025-12-11查看详情 > -
关于公开征求《化学药物残留溶剂的风险评估和控制的共性问题（征求意见稿）》意见的通知-2026/1/22
2026-01-23查看详情 > -
Document: Standard operating procedure for annual review of VeDDRA list to be used in EudraVigilance Veterinary-2026/2/26
2026-02-27查看详情 > -
Page: Pre-authorisation guidance-2026/3/27
2026-03-30查看详情 > -
Pulmonary Tuberculosis: Developing Drugs for Treatment-2026/5/8
2026-05-09查看详情 >
