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作 者:张庆平
机构地区:[1]浙江省义乌市中医医院,322000
出 处:《临床合理用药杂志》2014年第26期34-36,共3页Chinese Journal of Clinical Rational Drug Use
摘 要:目的为全面加强医疗机构的药品质量管理,完善医疗机构药品管理机制,保障临床用药安全提供安全参考。方法在查阅大量文献的基础上,进行归纳总结,介绍了医疗机构药品质量监督管理制度的历史变化以及药品监督管理现状,提出现阶段存在的相关问题并由此进行思考,分析问题存在的原因,并且提出一些合理的建议与对策。结果医疗机构的药品质量管理存在诸多问题,包括从业人员素质水平,药品购置、保养乃至对药品质量的监管与立法等。结论推行《药品经营质量管理规范》管理模式,把医疗机构药品质量监管纳入到法制化轨道。Objective To provide security reference For strengthening the management of the medical institution drug quality,perfecting drug management mechanism of medical institutions and guaranteeing clinical medication safety. Methods This article was based on a large number of documental materials. And on the basis of summarization of these materials,the paper introduced the history changes of the drug quality supervision and management of the medical institution system and the present situation of drug supervision and management,which put forward the existing problems,analyzed the causes of the existing problems,finally,came up with some reasonable suggestions and countermeasures. Results The drug quality management of medical institutions have many problems,including the staff quality level,drug purchase,maintenance and even to drug quality supervision and legislation. Conclusion The GSP management mode should be carried out,to make the medical institution drug quality supervision into legalized track,and make medical institutions drug store management more standard.we should imply GSP management mode,make the medical institution drug quality supervision into legalized track,to make medical institutions drug store management more standard.
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