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Document: Combined VeDDRA list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products-2025/8/12
2025-08-13查看详情 > -
药你知道 | 《国家药监局关于发布优化全生命周期监管支持高端医疗器械创新发展有关举措的公告》系列解读（八）-2025/9/26
2025-09-28查看详情 > -
Document: Member states contact points for review of national versions of the content of mobile scanning and other technologies-2025/11/4
2025-11-05查看详情 > -
Document: Classification of changes-2025/12/3
2025-12-04查看详情 > -
Clinical Decision Support Software-2026/1/6
2026-01-08查看详情 > -
关于将依维莫司微片纳入“儿童抗肿瘤药物研发鼓励试点计划（星光计划）”试点项目的通知-2026/2/12
2026-02-13查看详情 > -
Page: Plant testing strategy in the risk assessment for veterinary medicinal products - Scientific guideline-2026/3/20
2026-03-23查看详情 > -
Document: Minutes of the CVMP meeting 10-12 February 2026-2026/4/24
2026-04-27查看详情 > -
Document: Minutes of PRAC meeting on 7-10 April 2026-2026/6/8
2026-06-09查看详情 > -
Document: Terms of reference for the European Medicines Agency, Health Canada and United States Food and Drug Administration cluster on blood products-2026/7/17
2026-07-19查看详情 >
