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国家药监局药审中心关于印发《药品审评中心药物临床试验期间安全信息评估与风险管理工作程序（试行）》的通知-2023/11/3
2023-11-07查看详情 > -
Document: Minutes - HMA-EMA joint Big Data Steering Group teleconference - 11 December 2024-2025/1/14
2025-01-15查看详情 > -
Page: Type-IB variations: questions and answers-2025/2/18
2025-02-19查看详情 > -
Page: Good Manufacturing Practice (GMP) / Distribution Practice Practice (GDP) Inspectors Working Group-2025/3/27
2025-03-28查看详情 > -
Page: Regulatory acceptance of new approach methodologies (NAMs) to reduce animal use testing-2025/5/2
2025-05-06查看详情 > -
Document: CHMP-CAT - D80-210 Overview to final EPAR - Rev 06.25 Revamp-2025/6/12
2025-06-13查看详情 > -
Page: Type-II variations: questions and answers-2025/7/17
2025-07-18查看详情 > -
Page: Industry Standing Group meetings-2025/9/1
2025-09-02查看详情 > -
Document: Timetable: Companion diagnostic follow-up consultation-2025/10/3
2025-10-08查看详情 > -
关于将Vorasidenib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-2025/11/13
2025-11-14查看详情 >
