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国家药监局药审中心关于发布《阿司匹林肠溶片生物等效性研究技术指导原则》的通告（2022年第36号）-2022/10/9
2022-11-14查看详情 > -
Pharmacogenomic Data Submissions(Draft)-2023/03/17
2023-03-17查看详情 > -
关于公开征求《药物临床试验不良事件相关性评价技术指导原则（征求意见稿）》意见的通知-2023/9/26
2023-09-28查看详情 > -
Page: Fees payable to the European Medicines Agency-2025/1/6
2025-01-07查看详情 > -
Page: Supporting innovation-2025/2/11
2025-02-12查看详情 > -
Page: Applying for marketing authorisation: orphan medicines-2025/3/19
2025-03-20查看详情 > -
Document: Business process description for medical devices-2025/4/22
2025-04-23查看详情 > -
Document: Superseded - EMA/PDCO Summary Report on the review of the list of granted Class Waivers-2025/6/3
2025-06-04查看详情 > -
Document: Clinical Trial Information System (CTIS) - Sponsor handbook-2025/7/9
2025-07-10查看详情 > -
关于公开征求ICH《M4Q（R2）：人用药品注册通用技术文档：质量》指导原则草案意见的通知-2025/8/14
2025-08-15查看详情 >
