兽药GMP现场检查常见问题解析  

Analysis of common problems in on-site inspection of veterinary drug GMP

作　　者：李雄[1] 李晟[1] 冯小花[1] LI Xiong;LI Sheng;FENG Xiao-hua(Hunan Institute of Animal and Veterinary Science,Changsha 410131,PCR.)

机构地区：[1]湖南省畜牧兽医研究所,湖南长沙410131

出　　处：《湖南畜牧兽医》2023年第3期37-39,共3页Hunan Journal of Animal Science & Veterinary Medicine

摘　　要：文章对兽药GMP现场检查中企业存在的常见问题进行梳理汇总,从机构与人员、厂房与设施、设备、物料与产品、确认与验证、文件管理、产品销售与召回七个方面探讨了问题产生的原因,并提出了相应的改进建议,以期为企业更好地实施兽药GMP工作提供参考。The author combed and summarized the common problems existing in the veterinary drug GMP on-site inspection,and explored from seven aspects of institutions and personnel,facilities,equipment,materials and products,confirmation and verification,document management,product sales and recalls.The reason forthe problem and put forward corresponding improvements in order to provide a reference for enterprises to better implement the GMP work of veterinary drugs.

关 键 词：兽药GMP 现场检查 缺陷项目 

分 类 号：S851.66[农业科学—预防兽医学]