|
Title:
|
HOW CAN QUALITY REQUIREMENTS FOR MEDICAL
SOFTWARE BE SYSTEMATICALLY FULFILLED
BETTER? |
|
Author(s):
|
Karin Messer-Misak, Jeroen de Bruin and Sten Hanke |
|
ISBN:
|
978-989-8704-18-4 |
|
Editors:
|
Mário Macedo |
|
Year:
|
2020 |
|
Edition:
|
Single |
|
Keywords:
|
Software Quality Standards, Requirements Engineering, Medical Software Engineering |
|
Type:
|
Short |
|
First Page:
|
203 |
|
Last Page:
|
208 |
|
Language:
|
English |
|
Cover:
|
|
|
Full Contents:
|
click to dowload 
|
|
Paper Abstract:
|
Due to a variety of factors, among others medical and legislative requirements, the quality requirements on medical
software become increasingly demanding. Several quality standards and guidelines are already in place, e.g., ISO/IEC
s9126, 14598 and 25000 (SQaRE). However, there is a debate on whether these standards are not specific enough for
medical software. Furthermore, their effective application for requirement gathering, analysis and monitoring can be
difficult. In this paper, we propose a workflow for the application of the ISO/IEC 25010:2011 standard for the systematic
collection, analysis and evaluation of requirements for various stakeholders in order to systematically better fulfill quality
requirements on medical software. |
|
|
|
|
|
|
