摘要
药品质量主要由多方面因素共同保障,其中加强药品生产监督管理是确保药品质量的重点环节。PDCA是由美国著名质量管理学者戴明先生提出,是管理学中的一个通用模型,其中P为明确方针与目的 ,制定活动计划;D为具体动作;C是对执行结果进行检查,确定效果,探寻待解决的问题;A对检查结果进行处理,总结成功经验,反思失败经验,将制定的解决方案投入到下一个循环中,可以提高企业生产监督管理工作的有高效性与科学性。本文对PDCA循环在药物品生产监督管理中的应用情况进行综述,分析PDCA循环在药品生产监督管理中应用的必要性与方法,旨在为推进药品生产质量最优化提供有利的参考。
The quality of drugs is mainly guaranteed by many factors.Strengthening the supervision and management of drug production is the key link to ensure the quality of drugs.PDCA is proposed by Mr.Deming,a famous quality management scholar in the United States.It is a general model in management,in which P is a clear policy and purpose,set up an activity plan;D is a specific action;C is to check the results of the execution,determine the effect and explore the problems to be solved;A deals with the results of the inspection and summarizes the successful experience.Reflecting on the failure experience and putting the solution into the next cycle,we can improve the efficiency and scientificity of the production supervision and management.This article reviews the application of PDCA cycle in the supervision and management of drug products production,analyzes the necessity and methods of the application of PDCA cycle in the supervision and management of drug production,in order to provide a favorable reference for the optimization of the quality of drug production.
作者
代永娟
DAI Yongjuan(Special Equipment Department,Peony District Market Supervision Bureau of Heze City,Heze Shandong 274000,China)
出处
《中国卫生标准管理》
2018年第15期98-100,共3页
China Health Standard Management