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A secure IRB system for assisting the development of intelligent medical devices

机译:安全的IRB系统,用于辅助智能医疗设备的开发

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Considering the demand for improvement of monitoring the elders' states of health, various kinds of intelligent medical devices have been designed by health care industries recently. This paper, therefore, develops an integrated Institutional Review Board (IRB) system to connect to hospitals, clinics, manufacturers, and customers for sharing information, reducing administrative costs, and further improving the quality of intelligent medical devices design. Moreover, two efficient security protocols are designed to establish secure communications in our developed integrated IRB system for protecting sensitive and confidential information. Main contributions of our developed IRB system are listed below, (i) The developed system provides a similar expert system to assist the development of intelligent medical devices and instantaneous management of clinical trails, (ii) Information about clinical trials and knowledge, clinical professionals, and trail investigators can be well constructed and maintained as a knowledge base for improving quality and efficiency of future clinical trials, (iii) The system provides a standard operating process and project management for clinical trials, (iv) It is efficient in accessing to IRB certification, (v) The developed system allows or assists the trial investigators and manufactures to communicate and cooperate with one another via a platform, (vi) Secure communications can be established in our IRB system, and hence all sensitive and confidential information can be protected from being disclosed, (vii) It is secure against potential attacks while users login to the developed IRB system.
机译:考虑到对改善对老年人健康状况的监视的需求,近来保健行业已经设计了各种智能医疗设备。因此,本文开发了一个集成的机构审查委员会(IRB)系统,以连接到医院,诊所,制造商和客户,以共享信息,降低管理成本并进一步提高智能医疗设备设计的质量。此外,设计了两种有效的安全协议以在我们开发的集成IRB系统中建立安全通信,以保护敏感和机密信息。以下是我们已开发的IRB系统的主要贡献:(i)已开发的系统提供了类似的专家系统,以协助智能医疗设备的开发和临床试验的即时管理;(ii)有关临床试验和知识的信息,临床专业人员,可以很好地构建和维护调查研究人员,并将其作为知识库,以提高未来临床试验的质量和效率;(iii)该系统为临床试验提供标准的操作流程和项目管理;(iv)有效地使用IRB认证,(v)所开发的系统允许或协助试验研究者和制造商通过一个平台相互沟通和合作,(vi)可以在我们的IRB系统中建立安全的通信,因此可以保护所有敏感和机密信息(vii)在用户登录已开发的IRB系统时可以安全地防范潜在的攻击em。

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