摘要
为规范医院医用体外诊断试剂引进、采购、冷链管理、库房验收、供应商管理,该文通过在体外诊断试剂实际管理中总结的经验,分析体外诊断试剂管理工作中出现的问题及存在的缺陷,探讨如何进一步改进体外诊断试剂的管理模式,对原先较为滞后的管理模式提出改进意见及思考,提高管理的工作效率,为临床提供更安全可靠的试剂,保证临床使用体外诊断试剂诊断和治疗疾病的准确性,为患者提高更精确、更安全的医疗服务。
In order to regulate the introduction of medical hospital,in vitro diagnostic reagents procurement,cold chain management,warehouse inspection,suppliermanagement,through the in vitro diagnostic reagent summarized actual management experience,analysis of the problems in the management of in vitrodiagnostic reagents and defects,to discuss how to further improve the in vitro diagnostic reagent management mode,put forward the improvement the viewsand Thoughts on the original lagging management mode,improve management efficiency,to provide more safe and reliable for clinical reagents,to ensureaccuracy of the clinical use of in vitro diagnostic reagents for the diagnosis and treatment of disease,improve the more precise and safe medical service for patients.
作者
张晓洁
李佳凤
ZHANG Xiao-jie;LI Jia-feng(Fujian Provincial Maternity and Child Care Center,Fujian Fuzhou 350001)
出处
《中国医疗器械信息》
2017年第10期8-9,26,共3页
China Medical Device Information
关键词
体外诊断试剂
采购
冷链
管理
in vitro diagnostic reagent
procurement
cold chain
management
