DocumentCode
2208868
Title
Software Risk Analysis in Medical Device Development
Author
Lindholm, Christin ; Notander, Jesper Pedersen ; Höst, Martin
Author_Institution
Dept. of Comput. Sci., Lund Univ., Lund, Sweden
fYear
2011
fDate
Aug. 30 2011-Sept. 2 2011
Firstpage
362
Lastpage
365
Abstract
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.
Keywords
biomedical equipment; health care; hospitals; medical computing; risk analysis; safety-critical software; Sweden; computer systems; health-care; medical device development; safety-critical software development; software risk analysis; software risk management process; Biomedical monitoring; Estimation; Monitoring; Risk management; Safety; Software; medical device development; risk analysis; risk management; software development;
fLanguage
English
Publisher
ieee
Conference_Titel
Software Engineering and Advanced Applications (SEAA), 2011 37th EUROMICRO Conference on
Conference_Location
Oulu
Print_ISBN
978-1-4577-1027-8
Type
conf
DOI
10.1109/SEAA.2011.65
Filename
6068331
Link To Document