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浅谈多质量体系条件下质量文件的整合与制订
引用本文:黄小红,黄红坤,许惠英,饶子亮,唐小江.浅谈多质量体系条件下质量文件的整合与制订[J].实验动物科学,2015,32(1):45-47.
作者姓名:黄小红  黄红坤  许惠英  饶子亮  唐小江
作者单位:广东省医学实验动物中心
摘    要:摘要: 质量文件是实验室建设的重要软件内容之一。质量文件的高度整合与规范制订是实验室多个质量体系得以 同时顺利运行的关键。本文介绍了 CNAS、CMA、CMAF、GLP 质量体系及其对质量文件的要求,以及笔者所在实验 室结合实际对质量文件进行整合与制订,实现多个质量体系同时顺利运行的具体做法和经验。

关 键 词:质量文件  多质量体系  整合  制订  

On the Integration and the Development of the Quality System Under the Conditions of Multi-quality Documents
HUANG Xiao-hong;HUANG Hong-kun;XU Hui-ying;RAO Zi-liang;TANG Xiao-jiang.On the Integration and the Development of the Quality System Under the Conditions of Multi-quality Documents[J].Shiyan Dongwu Kexue,2015,32(1):45-47.
Authors:HUANG Xiao-hong;HUANG Hong-kun;XU Hui-ying;RAO Zi-liang;TANG Xiao-jiang
Institution:HUANG Xiao-hong;HUANG Hong-kun;XU Hui-ying;RAO Zi-liang;TANG Xiao-jiang;Guangdong medical laboratory animal center;
Abstract:Abstract:Quality document is an important software content of laboratory construction. Highly integrated and standardized quality documents is a key laboratory to develop a number of quality systems to simultaneously run smoothly. This article describes the CNAS,CMA,CMAF,GLP quality system and quality documentation requirements,as well as the author of the laboratory where the actual file on the quality of integration and the development,practice and experience to achieve a number of specific quality system simultaneously running smoothly.
Keywords:quality documents  multi-quality systems  integration  formulate  
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