首页 >
法规速递
-
国家药监局药审中心关于发布《抗体偶联药物非临床研究技术指导原则》的通告（2023年第46号）-2023/9/27
2023-09-28查看详情 > -
Document: Organisation chart: Information Management-2025/1/6
2025-01-07查看详情 > -
Page: Non-clinical Working Party-2025/2/11
2025-02-12查看详情 > -
Document: 2024 European Medicines Agency annual report on independence-2025/3/19
2025-03-20查看详情 > -
Document: Business process description for parallel distribution-2025/4/22
2025-04-23查看详情 > -
Document: EMA/PDCO summary report on the review of the list of granted Class Waivers 2 June 2025-2025/6/3
2025-06-04查看详情 > -
Document: Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, (Multi trial) substantial modification, non-substantial modification, and Request for information (RFI)-2025/7/9
2025-07-10查看详情 > -
国家药监局药审中心关于发布《骨关节炎新药临床研发技术指导原则》的通告（2025年第33号）-2025/8/14
2025-08-15查看详情 > -
Page: PRIME: priority medicines-2025/9/26
2025-09-28查看详情 > -
Page: Medical devices-2025/11/4
2025-11-05查看详情 >
