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Document: Minutes of the CAT meeting 5-7 November 2025-2026/1/27
2026-01-28查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2026/3/4
2026-03-05查看详情 > -
Document: Minutes of the COMP meeting 17-19 February 2026-2026/4/1
2026-04-02查看详情 > -
Document: Highlights from the third expert panels and notified bodies workshop-2026/5/18
2026-05-19查看详情 > -
国家药监局关于19批次药品不符合规定的通告（2022年第55号）-2022/11/15
2022-11-30查看详情 > -
国家药监局关于15批次药品不符合规定的通告（2023年第26号）-2023/6/20
2023-06-21查看详情 > -
Draft Guidance: Advanced Manufacturing Technologies Designation Program FDA Creates New Advisory Committee for Evaluation of Genetic Metabolic Disease Treatments-2023/12/12
2023-12-21查看详情 > -
Page: Parallel scientific advice processes and special product types-2025/1/22
2025-01-23查看详情 > -
Document: List of medicinal products under additional monitoring-2025/2/24
2025-02-25查看详情 > -
Document: Day 80 assessment report - Non-clinical template with guidance Rev. 03.25 - Revamp-2025/4/1
2025-04-02查看详情 >
