摘要
该文通过对2009年我省药品生产企业GMP认证现场检查中出现的主要缺陷项目进行分析,找出该省药品生产企业实施GMP的薄弱环节,为进一步加强GMP技术监督提供建议。
This article analysed the main defective items observed in GMP certification on-site inspection of pharmaceutical manufactures in Anhui province in 2009,to find out the weaknesses of pharmaceutical manufacturers in executing GMP.The opinion and advice of further enhancing GMP tech-administration were also proposed.
出处
《安徽医药》
CAS
2011年第2期243-244,共2页
Anhui Medical and Pharmaceutical Journal
关键词
GMP认证
缺陷项目
分析
GMP certification
defective items
analysis