Software risk analysis in medical device development

Christin Lindholm, Jesper Holmén Notander, Martin Höst

Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKonferenspaper i proceedingPeer review

Sammanfattning

The purpose of risk management in the development of safety-critical software is to eliminate or reduce harmful behaviour. In health-care it is essential to manage risk related to software due to its increased use in medical devices and other computer systems. This paper presents some of the experiences gained from an ongoing case study at a large hospital in Sweden. The study focuses on identification and analysis of risks using scenarios and how effective this approach is. The research is conducted as action research, with the aim of analysing and giving input to the organisation’s new software risk management process.
Originalspråkengelska
Titel på värdpublikationProceedings of the 37th EUROMICRO Conference on Software Engineering and Advanced Applications
RedaktörerStefan Biffel, Mika Koivuluoma, Pekka Abrahamsson, Markku Oivo
FörlagIEEE - Institute of Electrical and Electronics Engineers Inc.
Sidor362-365
Antal sidor4
ISBN (tryckt)978-0-7695-4488-5
StatusPublished - 2011
EvenemangEUROMICRO Conference on Software Engineering and Advanced Applications - Oulu, Finland
Varaktighet: 2011 aug. 302011 sep. 2

Konferens

KonferensEUROMICRO Conference on Software Engineering and Advanced Applications
Land/TerritoriumFinland
OrtOulu
Period2011/08/302011/09/02

Ämnesklassifikation (UKÄ)

  • Datavetenskap (datalogi)

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