A Roadmap to Implement a Quality Management System

Derek Flood, Fergal Mc Caffery, Valentine Casey


In recent years the proportion and complexity of software in medical devices has increased considerably. This has presented an opportunity for software development organisations to expand into the medical device domain. Due to the high level of risk associated with medical devices, strict regulations must be adhered to in order to market such products. One key aspect of these regulations is the necessity to have in place a Quality Management System to help ensure an organisations’ ability to consistently meet customer and regulatory requirements. This paper presents a roadmap which can be used to assist organisations, wishing to develop medical device software to implement a Quality Management System.


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Paper Citation

in Harvard Style

Flood D., Mc Caffery F. and Casey V. (2013). A Roadmap to Implement a Quality Management System . In Proceedings of the International Conference on Health Informatics - Volume 1: HEALTHINF, (BIOSTEC 2013) ISBN 978-989-8565-37-2, pages 133-138. DOI: 10.5220/0004183601330138

in Bibtex Style

author={Derek Flood and Fergal Mc Caffery and Valentine Casey},
title={A Roadmap to Implement a Quality Management System},
booktitle={Proceedings of the International Conference on Health Informatics - Volume 1: HEALTHINF, (BIOSTEC 2013)},

in EndNote Style

JO - Proceedings of the International Conference on Health Informatics - Volume 1: HEALTHINF, (BIOSTEC 2013)
TI - A Roadmap to Implement a Quality Management System
SN - 978-989-8565-37-2
AU - Flood D.
AU - Mc Caffery F.
AU - Casey V.
PY - 2013
SP - 133
EP - 138
DO - 10.5220/0004183601330138