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国家药监局药审中心关于发布《基因治疗血友病临床试验设计技术指导原则》的通告（2023年第29号）-2023/4/14
2023-04-14查看详情 > -
国家药监局药审中心关于发布《药物临床试验方案提交与审评工作规范》的通告（2023年第51号）-2023/10/13
2023-10-13查看详情 > -
Page: Procurement-2025/1/8
2025-01-09查看详情 > -
Document: Article 57 product data-2025/2/14
2025-02-18查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2025/3/25
2025-03-26查看详情 > -
Document: Agenda - Extraordinary Management Board meeting: 28 April 2025-2025/4/28
2025-04-29查看详情 > -
Document: QRD veterinary product-information highlighted template version 9.1-2025/6/5
2025-06-06查看详情 > -
Document: Agenda of the CVMP meeting 15-17 July 2025-2025/7/15
2025-07-16查看详情 > -
Document: Vaccine Monitoring Platform: List of EMA-funded studies-2025/8/21
2025-08-22查看详情 > -
Page: Quality of medicines questions and answers: Part 1-2025/9/30
2025-10-08查看详情 >
