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Document: Superseded - EMA/PDCO Summary Report on the review of the list of granted Class Waivers-2025/6/3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 > -
Document: Recommendations on eligibility to PRIME scheme adopted at the CHMP meeting of 15-18 September 2025-2025/9/26
2025-09-28查看详情 > -
Page: Combination Products Operational Group-2025/11/4
2025-11-05查看详情 > -
QTc Information in Human Prescription Drug and Biological Product Labeling-2025/12/3
2025-12-04查看详情 > -
国家药监局药审中心关于发布《境外生产药品上市后备案类变更办理程序》的通告（2026年第3号）-2026/1/9
2026-01-09查看详情 > -
Document: Organisation chart: Human Medicines-2026/2/12
2026-02-13查看详情 > -
Page: Good Manufacturing Practice (GMP) / Good Distribution Practice (GDP) Inspectors Working Group-2026/3/23
2026-03-24查看详情 > -
Document: European Shortages Monitoring Platform (ESMP): Implementation guide for marketing authorisation holders-2026/4/28
2026-04-29查看详情 >
