摘要
目的:介绍新增耗材审批制度并强调其必要性。方法:阐述审批制度的内容、流程以及实施过程中应注意的问题。结果:新增医用耗材审批制度,一方面可以使采购过程有据可依;另一方面引进必要的新产品,限制同类或淘汰不能适应的产品。结论:建立新增医用耗材审批制度,满足了临床需要,规范了采购工作程序和医院用械制度。
Objective To introduce the necessity of newly added examination and approval system. Methods The expatiation content of examination and approval system, process and the attention-getting problems of implementation were expounded. Results The new system is established, on the one hand it can be made evidence-based in the purchasing process and on the other hand it can be limited to same species and wash out inadaptable manufacture. Conclusion The newly added examination and approval system was built to meet the clinic need and conform to the standard of using equipment in hospital.
出处
《医疗卫生装备》
CAS
2009年第1期103-104,共2页
Chinese Medical Equipment Journal
关键词
医用耗材
新增审批
必要性
medical disposable
newly added examination and approval
necessity