摘要
中药材是中药产业的物质基础,稳定优质的中药材是中药饮片、中药制剂生产质量的保障,也是中医临床疗效发挥的根基。规范、标准和可溯源是中药材生产质量管理规范(GAP)对中药材基地生产的基本要求。文中通过对中药材GAP认证现场检查情况的统计和分析,探讨了中药材基地建设中普遍存在的问题和薄弱环节,并对中药材GAP基地建设及认证准备工作提出了意见和建议。
Chinese crude drugs is the basis of Traditional Chinese Medicines(TCM).The roles of artificial cultivation of main raw materials in preparing slices of Chinese crude drugs and TCM preparations have been realized.Standardized planting and industrialized production are now being developed step by step.In this article,we discussed the GAP on-site inspections,analyzed the deficiencies and weakness in GAP plant construction,and identified how to improve GAP implementation and make preparations for the inspection.
出处
《中国新药杂志》
CAS
CSCD
北大核心
2011年第2期106-109,128,共5页
Chinese Journal of New Drugs
关键词
中药材
中药材生产质量管理规范
现场检查
基地建设
Chinese crude drugs
good agricultural practice(GAP)
on-site inspection
GAP plant construction