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1.
Biomed Instrum Technol ; 48(1): 64-71, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24548041

RESUMEN

Medical device interoperability has been identified as a key way of decreasing healthcare costs while improving patient care. 1 This has led to a shift toward placing more medical devices onto information technology (IT) networks. However, placing medical devices onto an IT network may lead to additional risks to safety, effectiveness and security of the devices, the network, and the data. ANSI/AAMI/IEC 80001-1 addresses the roles, responsibilities, and activities that need to be carried out when managing these risks. In this article, we describe an exercise undertaken to assess the medical IT network risk management practice implemented within a hospital to control risk associated with a clinical information system (CIS). The level of compliance with the 80001-1 standard was determined using an assessment framework developed by the Regulated Software Research Centre. The purpose of this exercise was to test and inform the development of an assessment method that is part of the assessment framework for this standard. The exercise also sought to identify how the management of such an existing CIS project meets the requirements of 80001-1.


Asunto(s)
Ingeniería Biomédica/normas , Redes de Comunicación de Computadores/normas , Guías de Práctica Clínica como Asunto , Gestión de Riesgos/normas , Administración de la Seguridad/normas , Estados Unidos
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