摘要
目的:为食品药品检测实验室(以下简称"实验室")管理体系文件的制订提供参考。方法:结合实验室自身的实际,从理论到实际对管理体系文件编制依据、层次结构、各层次文件具体内容进行分析和探讨。结果:明确了编制依据的整合方法、体系文件的层次结构和文件具体内容。结论:实验室应做好需求分析,解决好文件编制依据、层次结构和文件具体内容等问题,才能编制科学实用、协调统一的管理体系文件。
Objective: To provide references for the formulation of management system documentation of food and drug-control laboratories. Methods: Combined with laboratorial condition, the compilation basis of management system documents, the structure of hierarchy, and the specific contents of each type of documents were analyzed and discussed from the aspects of theory and practice. Results: The integration methods of compilation basis, the hierarchical structure of system documents and the specific contents of files were clarified. Conclusion: The laboratory should analyze the demands, solve problems such as compilation basis, hierarchical structure and specific contents, so as to prepare the scientific, practical, consistent and unified management system documents.
出处
《中国药事》
CAS
2015年第11期1141-1144,共4页
Chinese Pharmaceutical Affairs
关键词
食品
药品
实验室
管理体系文件
food
drug
laboratory
management system document