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Document: List of changes to combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animal and humans to veterinary medicinal products for 2025-2025/7/31
2025-08-01查看详情 > -
国家药监局综合司公开征求《国家药监局关于深化化妆品监管改革促进产业高质量发展的意见 （征求意见稿）》意见-2025/9/19
2025-09-22查看详情 > -
关于将盐酸阿思尼布片/胶囊装微片纳入《儿童抗肿瘤药物研发鼓励试点计划（星光计划）》试点项目的公示-2025/10/27
2025-10-28查看详情 > -
Page: Extensions of marketing authorisations: questions and answers-2025/11/26
2025-11-27查看详情 > -
Document: Technology Capability Investment Plan to 2028 - Becoming a digital hub for the European medicines regulator network-2025/12/19
2025-12-22查看详情 > -
Page: Epidemiological data on blood transmissible infections - Scientific guideline-2026/2/4
2026-02-05查看详情 > -
Document: Concept paper on the development of a reflection paper on proof-of-concept data to support the development of anti-cancer medicinal products in paediatric patients-2026/3/13
2026-03-16查看详情 > -
国家药监局药审中心关于发布《以患者为中心的中药新药临床研发技术指导原则》的通告（2026年第29号）-2026/4/13
2026-04-14查看详情 > -
Document: European Medicines Agency’s privacy statement for legal entity and bank account validation-2026/5/28
2026-05-29查看详情 > -
Regulatory and procedural guideline: Information note on the format and validity features of electronic certificates for medicines issued by the European Medicines Agency (updated)-2023/01/16
2023-01-16查看详情 >
