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Document: QRD Form 2 and checklist for the submission of day +25 files - veterinary-2025/11/4
2025-11-05查看详情 > -
Page: Eligible healthcare professionals' organisations-2025/12/3
2025-12-04查看详情 > -
Document: European Medicines Agency budget for 2026-2026/1/8
2026-01-09查看详情 > -
国家药监局综合司关于印发2026年医疗器械行业标准制修订计划项目的通知-2026/2/12
2026-02-13查看详情 > -
Document: MedDRA important medical event terms list - version 29.0-2026/3/20
2026-03-23查看详情 > -
关于公开征求《硼中子俘获治疗药物临床研发技术指导原则（征求意见稿）》意见的通知-2026/4/28
2026-04-29查看详情 > -
国家药监局药审中心关于发布《化学仿制药口服调释制剂乙醇剂量倾泻试验药学研究技术指导原则》的通告（2022年第38号）-2022/11/8
2022-11-14查看详情 > -
Definitions of Suspect Product and Illegitimate Product for Verification Obligations Under the Drug Supply Chain Security Act Guidance for Industry(Final)-2023/03/16
2023-03-16查看详情 > -
国家药监局综合司关于同意吉林省药品检验研究院增加生物制品批签发证明文件授权签发人的复函-2023/9/27
2023-09-28查看详情 > -
Document: Annex to interim measures regarding notification of pharmacovigilance alerts by marketing authorisation holders under Regulation (EU) 2019/6: contact points-2025/1/6
2025-01-07查看详情 >
