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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 > -
Document: Data protection notice for legal entity and bank account validation regarding payments-2026/6/8
2026-06-09查看详情 > -
Document: Dual chamber leadless pacemaker - Notified Bodfy 123 - 28/03/2024 - Expert decision and opinion in the context of the clinical evaluation consultation procedure (CECP)-2026/7/17
2026-07-19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 >
