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关于公开征求《药物临床试验生物样品分析实验室合规性回顾报告（征求意见稿）》意见的通知-2026/4/29
2026-04-30查看详情 > -
阿司匹林肠溶片生物等效性研究技术指导原则-2022/10/9
2022-11-14查看详情 > -
Draft Guidance: Patient-Focused Drug Development: Incorporating Clinical Outcome Assessments Into Endpoints for Regulatory Decision-Making-2023/4/5
2023-04-06查看详情 > -
Regulatory and procedural guideline: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure (updated)-2023/9/29
2023-10-07查看详情 > -
Page: EudraVigilance training and support-2025/1/7
2025-01-08查看详情 > -
国家药监局综合司公开征求《康复类数字疗法软件产品分类界定指导原则（征求意见稿）》意见-2025/2/12
2025-02-14查看详情 > -
Page: Medical devices-2025/3/24
2025-03-25查看详情 > -
Page: Procurement-2025/4/23
2025-04-24查看详情 > -
Document: IVF Media G5 - Procedural steps and scientific information after initial consultation-2025/6/4
2025-06-05查看详情 > -
Page: Fees payable to the European Medicines Agency: General questions and answers-2025/7/10
2025-07-11查看详情 >
