Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Dorling, Alec"'
Autor:
Clarke, Paul, Lepmets, Marion, McCaffery, Fergal, Finnegan, Anita, Dorling, Alec, Flood, Derek
In the main, software development is a business which is frequently challenged with quality concerns, with the overwhelming majority of software users having experienced some level of difficulty using software at some point in time. One of the primar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2656::a1e12b965248def50518674ad69b4f37
http://eprints.dkit.ie/404/
http://eprints.dkit.ie/404/
Autor:
Clarke, Paul, Lepmets, Marion, Mc Caffery, Fergal, Finnegan, Anita, Dorling, Alec, Eagles, Sherman
peer-reviewed This paper aims to describe the software development settings of medical device domain focusing on the demands of the safety critical software processes. Medical device software developers have to adhere to a number of regulations and s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::dc00c096a3e98642dbd88eae6a57998b
http://eprints.dkit.ie/400/
http://eprints.dkit.ie/400/
Software that is incorporated into a medical device, or which is a standalone medical device in its own right, is of a safety critical nature and subject to regulation from various jurisdictions (principally the EU and the US). In order to satisfy ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2656::ef9317011c8298fa1d516b99adb9be85
http://eprints.dkit.ie/402/
http://eprints.dkit.ie/402/
Autor:
Dorling, Alec, Mc Caffery, Fergal
peer-reviewed Abstract. Process Improvement has been used for decades as a means to become better and more efficient. Whilst many organizations have used considerable resources for process improvement, investments in process improvement have not alwa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1249::aebecb417680a860318844514324f603
Autor:
McCaffery, Fergal, Dorling, Alec
This paper outlines the development of a software process assessment and improvement model (Medi SPICE) for the medical device industry. The paper details how medical device regulations may be satisfied by extending relevant processes and practices f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2656::6f7dd8af32e2b5eca240610f474b5516
http://eprints.dkit.ie/194/
http://eprints.dkit.ie/194/