| 陆德,裴宇盛,臧克承,肖妍.基于警告信对美国FDA远程监管评估的探讨分析[J].中国药事,2024,38(8):961-968 |
| 基于警告信对美国FDA远程监管评估的探讨分析 |
| Analysis of FDA's Remote Regulatory Assessments based on Warning Letters |
| 投稿时间：2024-04-18 |
| DOI：10.16153/j.1002-7777.20240307 |
| 中文关键词: 远程监管评估 远程交互评估 警告信 药品生产质量管理规范 质量管理体系 |
| 英文关键词: remote regulatory assessments remote interactive evaluations warning letters good manufacturingpractice for drugs quality management system |
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| 中文摘要: |
| 目的：介绍FDA发布的远程监管评估相关指南，并结合基于远程监管评估发布的警告信进行分析，为行业提供参考。方法：介绍FDA发布的远程监管评估指南及远程交互评估指南，并基于远程监管评估发布的警告信，从缺陷情况以及发布警告信的时间方面进行分析，提出参考建议。结果：FDA基于远程监管评估发布的警告信与现场检查发布的警告信相比，其缺陷条款以及发布时间上均有特点。结论：远程监管评估作为一种新的监管工具，有其独特的优势和不足之处，给监管部门以及药品生产企业均带来新的挑战。 |
| 英文摘要: |
| Objective: To introduce the relevant guidlines for remote regulatory assessments issued by FDA andanalyze the warning letters issued based on remote regulatory assessments to provide references for the industry.Methods: This paper introduced the remote interactive evaluations guidelines and remote regulatory assessmentsguidelines issued by FDA, and analyzed the warning letters issued based on remote regulatory assessmentsfrom the aspects of defects and the time of issuing warning letters, and put forward reference opinions. Results:Warning letters issued by the FDA based on remote regulatory assessments have unique characteristics in terms ofdefect terms and timing compared to warning letters issued by inspections. Conclusion: As a new regulatory tool,remote regulatory assessments has its unique advantages and disadvantages, and it also brings new challenges toboth regulatory authorities and pharmaceutical manufacturers. |
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