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Document: Concept paper on the revision of the guidelines on Good Manufacturing Practice for medicinal products - Annex 15 - Qualification and validation - Corrigendum-2026/7/15
2026-07-16查看详情 > -
国家药监局药审中心关于发布《放射性体内治疗药物临床评价技术指导原则》的通告（2023年第9号）-2023/02/15
2023-02-15查看详情 > -
Final Guidance: Nontuberculous Mycobacterial Pulmonary Disease Caused by Mycobacterium avium Complex: Developing Drugs for Treatment-2023/9/1
2023-09-04查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第八十八批）的通告（2025年第1号）-2025/1/6
2025-01-06查看详情 > -
Page: Submission deadlines for orphan designations-2025/2/6
2025-02-10查看详情 > -
Document: User guide for micro, small and medium-sized enterprises-2025/3/14
2025-03-17查看详情 > -
Page: Fees payable to the European Medicines Agency: Annual fees and remuneration-2025/4/15
2025-04-16查看详情 > -
2025年5月30日中药品种保护受理公示 -2025/5/30
2025-05-30查看详情 > -
Page: CHMP opinions on consultation procedures-2025/7/2
2025-07-03查看详情 > -
Page: Scientific Advisory Group on Immune and Inflammatory Diseases-2025/8/5
2025-08-06查看详情 >
