论植入性医疗器械临床流通规范化全过程管理  

The View of Entire Process Normalized Management of Implantable Medical Device in Clinical Circulation

作　　者：李晓刚[1] 李萍[1] 王贤喜[1] 孙天庭 

机构地区：[1]上海市东方医院,上海200120

出　　处：《中国医疗器械信息》2007年第8期57-59,共3页China Medical Device Information

摘　　要：如何对植入性医疗器械临床流通过程进行规范管理一直是困绕医院管理者的话题。我院通过开展全过程医疗质量实时监控,规范了植入性医疗器械从购销、使用、随访整个临床流通过程的管理,充分保障了患者用械安全。How to do the normalized entire process management of implantable medical device in clinical circulating is a topic troubling hospital administrator for a long time. Our hospital normalizes the entire process management of medical implantable instruments, which including the purchasing, the clinical using, and the fellow-up, through real-time monitoring the medical quality, guaranteeing patients＇ security in using the instruments.

关 键 词：植入性医疗器械 医疗质量 实时监控 

分 类 号：F203[经济管理—国民经济]