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Page: Quality of medicines questions and answers: Part 2-2026/1/30
2026-02-02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-2026/3/10
2026-03-11查看详情 > -
Document: Veterinary medicine safety day: How to check veterinary medicines are working-2026/4/8
2026-04-09查看详情 > -
关于更新PDF文件批量电子签章软件的通知-2023/01/03
2023-01-03查看详情 > -
关于公开征求《申报资料电子光盘技术要求(征求意见稿)》等文件意见及发布电子申报资料制作软件试用版的通知-2023/7/7
2023-07-10查看详情 > -
关于境外生产药品证明文件有关事宜的通知-2024/1/23
2024-02-05查看详情 > -
Document: List of medicinal products under additional monitoring-2025/1/29
2025-02-05查看详情 > -
Document: Vitrolife IVF media - Procedural steps and scientific information after initial consultation-2025/3/5
2025-03-06查看详情 > -
Page: Animal health practitioners-2025/4/8
2025-04-09查看详情 > -
Document: European Medicines Agency’s Data Protection Notice for the Organisation Management System (OMS) activities-2025/5/19
2025-05-20查看详情 >
