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Browsing by Author "Coleman, Gerry"

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Browsing by Author "Coleman, Gerry"

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  • Mc Caffery, Fergal; Casey, Valentine; Sivakumar, M.S.; Coleman, Gerry; Donnelly, Peter; Burton, John (Springer Verlag, 2012)
    Software traceability is central to medical device software develop-ment and essential for regulatory approval. In order to comply with the regulatory requirements of the medical device industry it is essential to have ...
  • Mc Caffery, Fergal; Coleman, Gerry (Praise Worthy Prize S.r.l., 2007)
    Software is becoming an increasingly important aspect of medical devices and medical device regulation. Software enables highly complex systems to be built. However, complexity is the enemy of safety, therefore strict ...
  • Coleman, Gerry; O'Connor, Rory V. (Springer, 2006)
    This paper presents the results of a Grounded Theory study of how software process and software process improvement (SPI) is applied in the practice of software development. This study described in this paper focused ...
  • McAnallen, Martin; Coleman, Gerry (EuroSPI, 2005)
    Updating and maintaining legacy systems creates significant challenges for software developers. Modifying legacy applications can be a time-consuming process which is fraught with architectural and code minefields. In many ...
  • Sivakumar, M.S.; Casey, Valentine; Mc Caffery, Fergal; Coleman, Gerry (2011)
    Effective verification and validation are central to medical device software de-velopment and are essential for regulatory approval. Although guidance is available in mul-tiple standards in the medical device software ...

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