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Page: Procurement-2025/2/7
2025-02-10查看详情 > -
Page: Contacts at the European Medicines Agency-2025/3/14
2025-03-17查看详情 > -
Page: ICH M15 guideline on general principles for model-informed drug development - Step 2b - Scientific guideline-2025/4/16
2025-04-16查看详情 > -
Document: Reflection paper on the application of Article 40(5) of Regulation (EU) 2019/6 for certain categories of variations-2025/6/2
2025-06-03查看详情 > -
关于公开征求药品电子通用技术文档（eCTD）相关技术文件和申报资料目录层级对应表意见的通知-2025/7/4
2025-07-07查看详情 > -
Document: Ketoprofen: European public maximum-residue-limit assessment report (EPMAR) - CVMP-2025/8/6
2025-08-07查看详情 > -
Document: Timetable: Post-authorisation measure (PAM) Paediatric art. 46 submission - ATMP-2025/9/24
2025-09-25查看详情 > -
Page: One Health approach-2025/11/3
2025-11-04查看详情 > -
Document: Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746)-2025/12/2
2025-12-03查看详情 > -
国家药监局关于加强药品受托生产监督管理工作的公告（2025年第134号）-2026/1/6
2026-01-07查看详情 >
