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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 > -
关于公开征求《慢性肾脏病治疗药物临床试验技术指导原则》意见的通知-2022/11/16
2022-11-25查看详情 > -
关于公开征求ICH《Q12：药品生命周期管理的技术和监管考虑》实施建议意见的通知-2023/4/26
2023-04-28查看详情 > -
Regulatory and procedural guideline: Procedural advice for orphan medicinal product designation: Guidance for sponsors (updated)-2023/10/20
2023-11-07查看详情 >
