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中药材生产质量管理规范延伸检查的实践与思考

徐贻权 莫结丽 严振 曾祥卫 欧阳蒲月 赖盼 郑聪敏

中国食品药品监管Issue(2):118-127,10.
中国食品药品监管Issue(2):118-127,10.DOI:10.3969/j.issn.1673-5390.2025.02.012

中药材生产质量管理规范延伸检查的实践与思考

Practice and Reflection on Extended Inspection Under Good Agricultural Practice for Chinese Crude Drugs

徐贻权 1莫结丽 2严振 2曾祥卫 1欧阳蒲月 3赖盼 1郑聪敏1

作者信息

  • 1. 广东省药品监督管理局审评认证中心
  • 2. 广东省药品监督管理局
  • 3. 广东食品药品职业学院
  • 折叠

摘要

Abstract

Ensuring the"six unifications",controlling key factors affecting the production and quality of Chinese medicinal materials,standardizing the entire production process,and achieving full traceability across the supply chain are core principles of good agricultural practice(GAP)for traditional Chinese medicine(TCM).This paper presents an analysis of GAP extended inspections conducted in Guangdong Province,focusing on key inspection aspects and processes.It highlights best practices,common challenges,and critical issues in GAP base construction and offers recommendations for improvement.A well-structured and appropriately invested GAP base,supported by a standardized operating model,is essential to ensuring stable,controllable,safe,and effective TCM quality.Strengthening GAP implementation and base development is crucial for sustainable industry growth,improving supply chain quality management,and promoting the high-quality development of the TCM industry.

关键词

中药材/生产质量管理规范/延伸检查/广东省/工作思考

Key words

Chinese crude drugs/good agricultural practice/extended inspection/Guangdong Province/work reflections

分类

医药卫生

引用本文复制引用

徐贻权,莫结丽,严振,曾祥卫,欧阳蒲月,赖盼,郑聪敏..中药材生产质量管理规范延伸检查的实践与思考[J].中国食品药品监管,2025,(2):118-127,10.

中国食品药品监管

1673-5390

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