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How to Prepare a Pre-Request for Designation (Pre-RFD)-2025/11/6
2025-11-07查看详情 > -
Document: All languages - Annex to the European Commission guideline on ‘Excipients in the labelling and package leaflet of medicinal products for human use’ (SANTE-2017-11668) - Revision 5-2025/12/5
2025-12-08查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2026/1/15
2026-01-16查看详情 > -
Document: HMA-EMA joint Network Data Steering Group meeting - 13 January 2026-2026/2/16
2026-02-26查看详情 > -
Page: Academia-2026/3/24
2026-03-25查看详情 > -
Document: Vaccine confidence advisory group: Terms of reference-2026/4/29
2026-04-30查看详情 > -
关于公开征求《阻塞性睡眠呼吸暂停治疗药物临床试验技术指导原则（征求意见稿）》意见的通知-2026/6/12
2026-06-12查看详情 > -
Review of Drug Master Files in Advance of Certain ANDA Submissions Under GDUFA (Draft)-2022/10/3
2022-11-14查看详情 > -
抗肿瘤抗体偶联药物临床研发技术指导原则-2023/4/7
2023-04-10查看详情 > -
关于公开征求《注射用醋酸亮丙瑞林微球生物等效性研究技术指导原则（征求意见稿）》意见的通知-2023/10/08
2023-10-08查看详情 >
