本文介绍了资质审核中针对不同类别的医疗器械供应商需要提交的资质证件,并说明了采购前和验货时资质审核的内容,最后提出了应用物流管理系统对供应商资质证件进行信息化管理。通过加强医疗器械资质审核的管理,确保临床使用的各类产品的合法性、有效性及安全性,有效减少医疗纠纷,对医院的持续健康发展起到了促进作用。%This paper introduced the qualiifcation documents that should be submitted by the suppliers of each kind of medical equipment and the information that ought to be verified before procurement and during the acceptance of medical equipment. Then, application of the logistics management system was suggested for informatization management of qualification documents of medical equipment, which can ensure the compliance, effectiveness and security of various medical equipment in its clinical applications. Additionally, this practice contributed to effective reduction of medical disputes and sustainable development of the hospital.
展开▼