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Malaria: Developing Drugs for Treatment-2025/9/23
2025-09-23查看详情 > -
Document: Agenda - ACT EU multi-stakeholder platform annual meeting - October 2025-2025/10/28
2025-10-29查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/11/28
2025-12-01查看详情 > -
国家药监局综合司公开征求《化妆品新原料注册备案资料管理规定（修订草案征求意见稿）》意见-2025/12/26
2025-12-29查看详情 > -
Document: Agenda - Webinar on the use of platform technologies in the non-clinical and clinical domains-2026/2/6
2026-02-09查看详情 > -
Document: Release notes - production release version 1.7.2615 March 2026 - Veterinary Medicinal Products Regulation: Union Product Database-2026/3/16
2026-03-17查看详情 > -
Page: Applying for orphan designation-2026/4/16
2026-04-17查看详情 > -
国家药监局药审中心关于发布《预防用mRNA疫苗临床试验技术指导原则（试行）》的通告（2026年第38号）-2026/6/1
2026-06-02查看详情 > -
关于公开征求《真实世界证据支持已上市药品扩展儿童适应症的沟通交流技术指导原则（征求意见稿）》意见的通知-2026/7/14
2026-07-15查看详情 > -
国家药监局关于发布《药物非临床研究质量管理规范认证管理办法》的公告（2023年第15号）-2023/01/19
2023-01-19查看详情 >
