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Regulatory and procedural guideline: European Medicines Agency procedural advice on recommendations on unforeseen variations according to Article 5 of Commission Regulation (EC) No 1234/2008-2023/5/31
2023-06-01查看详情 > -
国家药监局药审中心关于发布《新药临床安全性评价技术指导原则》的通告（2023年第59号）-2023/12/1
2023-12-04查看详情 > -
Document: Agenda - Medicine Shortages (SPOC) Working Party 21 January 2025-2025/1/21
2025-01-22查看详情 > -
Page: Pre-authorisation guidance-2025/2/24
2025-02-25查看详情 > -
Document: Procedural guidance to scientific committeesꞌ members and experts on completing the European Medicines Agencyꞌs declaration of interests in the Experts Management Tool-2025/4/1
2025-04-02查看详情 > -
关于电子申报资料网络传输系统升级维护的通知-2025/5/9
2025-05-12查看详情 > -
Document: Superseded list of references supporting the assessment of Zingiber officinale Roscoe, rhizoma-2025/6/19
2025-06-20查看详情 > -
Document: HMA-EMA joint Network Data Steering Group meeting - 28 May 2025-2025/7/24
2025-07-25查看详情 > -
Document: Agenda of the CVMP meeting 9-11 September 2025-2025/9/8
2025-09-09查看详情 > -
Document: Presentation - The summary-of-product-characteristics guideline and paediatric aspects-2026/10/10
2025-10-11查看详情 >
