{"title":"根据医疗器械的规定生产高质量的软件","authors":"S. B. Leif, R. Leif","doi":"10.1109/CBMS.1992.244939","DOIUrl":null,"url":null,"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.<<ETX>>","PeriodicalId":197891,"journal":{"name":"[1992] Proceedings Fifth Annual IEEE Symposium on Computer-Based Medical Systems","volume":"4 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1992-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Producing quality software according to medical regulations for devices\",\"authors\":\"S. B. Leif, R. Leif\",\"doi\":\"10.1109/CBMS.1992.244939\",\"DOIUrl\":null,\"url\":null,\"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.<<ETX>>\",\"PeriodicalId\":197891,\"journal\":{\"name\":\"[1992] Proceedings Fifth Annual IEEE Symposium on Computer-Based Medical Systems\",\"volume\":\"4 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1992-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"[1992] Proceedings Fifth Annual IEEE Symposium on Computer-Based Medical Systems\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/CBMS.1992.244939\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"[1992] Proceedings Fifth Annual IEEE Symposium on Computer-Based Medical Systems","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/CBMS.1992.244939","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Producing quality software according to medical regulations for devices
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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