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Final Guidance: Reformulating Drug Products That Contain Carbomers Manufactured With Benzene-2023/12/27
2024-01-03查看详情 > -
Recommendations to Reduce the Risk of Transmission of Disease Agents Associated with Sepsis by Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)-2025/1/31
2025-02-05查看详情 > -
Document: Guidance on the details of the classification of variations requiring assessment according to Article 62 of Regulation (EU) 2019/6 for veterinary medicinal products and on the documentation to be submitted pursuant to those variations-2025/2/27
2025-03-03查看详情 > -
Document: Highlight report - 13th Industry stakeholder platform on research and development support-2025/4/4
2025-04-07查看详情 > -
Document: HMPC: overview of assessment work - priority list-2025/5/15
2025-05-16查看详情 > -
2025年6月25日中药品种保护受理公示-2025/6/25
2025-06-26查看详情 > -
Document: Template for scientific document for paediatric investigation plan or product-specific waiver-2025/7/28
2025-07-29查看详情 > -
关于公开征求《艾滋病免疫功能重建不全治疗药物临床试验技术指导原则(征求意见稿)》意见的通知-2025/9/12
2025-09-12查看详情 > -
Document: Process for the electronic submission of medicinal product information - Chapter 3-2025/10/16
2025-10-17查看详情 > -
国家药监局关于发布药品生产企业出口药品检查和出口证明管理规定的公告(2025年第113号)-2025/11/21
2025-11-24查看详情 >