Discussion on Strengthening the Hospital Management of in Vitro Diagnostic Reagents

This article explored practical management experience of in vitro diagnostic reagents, continuously improved the informatization of in vitro diagnostic reagents and carried out cost-benefit analysis further, through studying "in vitro diagnostic reagents Registration" issued by China Food and Drug Administration in 2014. So that we achieved a unified centralized management of in vitro diagnostic reagents, improved the working efficiency and provided patients with more accurate and efficient service.