Producing quality software according to medical regulations for devices

S. B. Leif, R. Leif
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引用次数: 5

Abstract

The US Food and Drug Administration and the European Community, through EC Directives, are requiring good manufacturing standards to be applied to the software development process. The creation of software is no longer to be treated as an art form, but as an engineering process. Previous descriptions of this process, as described by US MIL-STD 2167A or the IEEE guidelines, are applicable to the software development process for medical instruments. A brief description of this methodology is given, and the suitability of the Department of Defense methodology, including the Ada programming language, for developing medical device software is discussed.<>
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根据医疗器械的规定生产高质量的软件
美国食品和药物管理局和欧洲共同体,通过欧盟指令,要求在软件开发过程中应用良好的制造标准。软件的创造不再被视为一种艺术形式,而是作为一个工程过程。美国MIL-STD 2167A或IEEE指南对该过程的先前描述适用于医疗器械的软件开发过程。简要介绍了该方法,并讨论了国防部方法的适用性,包括Ada编程语言,用于开发医疗设备软件。
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