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Development of the Medi SPICE PRM

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Show simple item record Casey, Valentine Mc Caffery, Fergal 2012-08-09T09:13:40Z 2012-08-09T09:13:40Z 2012
dc.description peer-reviewed en_US
dc.description.abstract As the importance and complexity of medical device software continues to increase there is growing demand for effective process assessment and improvement in this domain. To address this need the Medi SPICE process assessment and improvement model is being developed. Regulatory compliance is both an important and challenging aspect of medical device software development. Particularly as new regulations are being released and existing standards revised due to the attention that software is receiving within the health domain. To comply with these latest developments the Medi SPICE Process Reference Model (PRM) is being developed to conform with ISO/IEC 12207:2008 and the forthcoming release of ISO/IEC 15504-5 (currently under ballot). This paper outlines the development of the Medi SPICE PRM. It also provides details of the schedule for the full release of the Medi SPICE model. en_US
dc.language.iso eng en_US
dc.publisher Springer en_US
dc.relation.ispartofseries Software Process Improvement and Capability dEtermination (SPICE), Communications in Computer and Information Science;290(8), pp. 265-268
dc.rights The original publication is available at en_US
dc.subject medical device software en_US
dc.subject software process improvement en_US
dc.subject SPI en_US
dc.subject ISO/IEC 15504-5: 2006 en_US
dc.subject SPICE 1SO/IEC12207:2008 en_US
dc.title Development of the Medi SPICE PRM en_US
dc.type info:eu-repo/semantics/conferenceObject en_US
dc.type.supercollection all_ul_research en_US
dc.type.supercollection ul_published_reviewed en_US
dc.contributor.sponsor SFI en_US
dc.relation.projectid 07/SK.I1299 en_US
dc.relation.projectid 08/IN.1/I2030 en_US
dc.relation.projectid 10/CE/I1855 en_US
dc.rights.accessrights info:eu-repo/semantics/openAccess en_US

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