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2018 | OriginalPaper | Buchkapitel

Association-Based Process Integration for Compliance with Core Standards in Development of Medical Software

verfasst von : DongYeop Kim, Ye-Seul Park, Byungjeong Lee, Jung-Won Lee

Erschienen in: Advances in Computer Science and Ubiquitous Computing

Verlag: Springer Singapore

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Abstract

Several standards for medical software require systematic development to ensure safety and performance. Core standards for medical software include IEC 60601-1, IEC 62034, and ISO 14971. And they present different activities. In this case, standards consist of contents related to development by referring to contents of one another. Therefore, it is difficult for a developer to identify reference-relationships with other standards for complying with one standard. For this, there are rules and studies that assist in the reference-association, but they do not provide the requirements at a view of developer. Therefore, we propose an integrated process to comply with the core standards. The proposed process is defined by analyzing the relationship between development process and so on. Then it includes the requirements and artifacts at each stage of the integrated process. This enables systematic development of medical software by providing the activities and requirements in terms of developer’s view.

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Literatur
1.
Zurück zum Zitat IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety and essential performance (2005) IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety and essential performance (2005)
2.
Zurück zum Zitat ISO 14971:2007, Medical devices - Application of risk management to medical devices ISO 14971:2007, Medical devices - Application of risk management to medical devices
3.
Zurück zum Zitat IEC 62304:2015.6, Medical device software - Software life cycle processes (2015) IEC 62304:2015.6, Medical device software - Software life cycle processes (2015)
4.
Zurück zum Zitat OD-2044 Ed. 2.2. – Evaluation of Risk Management in Medical electrical equipment according to the IEC 60601-1 & IEC/ISO 80601-1 Series of Standards (2013) OD-2044 Ed. 2.2. – Evaluation of Risk Management in Medical electrical equipment according to the IEC 60601-1 & IEC/ISO 80601-1 Series of Standards (2013)
5.
Zurück zum Zitat Clarke, P., Lepmets, M., McCaffery, F., Finnegan, A., Dorling, A., Eagles, S.: Characteristics of a medical device software development framework. In: EuroSPI (2014) Clarke, P., Lepmets, M., McCaffery, F., Finnegan, A., Dorling, A., Eagles, S.: Characteristics of a medical device software development framework. In: EuroSPI (2014)
6.
Zurück zum Zitat Lepmets, M., Clarke, P., McCaffrey, F., Finnegan, A.: Development of a process assessment model for medical device software development. In: EuroSPI, Luxembourg, June 2014 Lepmets, M., Clarke, P., McCaffrey, F., Finnegan, A.: Development of a process assessment model for medical device software development. In: EuroSPI, Luxembourg, June 2014
7.
Zurück zum Zitat Kim, D.Y., Park, Y.S., Lee, J.W.: Development life cycle-based association analysis of requirements for risk management of medical device software. In: KIPS, Jeju, April 2017 Kim, D.Y., Park, Y.S., Lee, J.W.: Development life cycle-based association analysis of requirements for risk management of medical device software. In: KIPS, Jeju, April 2017
Metadaten
Titel
Association-Based Process Integration for Compliance with Core Standards in Development of Medical Software
verfasst von
DongYeop Kim
Ye-Seul Park
Byungjeong Lee
Jung-Won Lee
Copyright-Jahr
2018
Verlag
Springer Singapore
DOI
https://doi.org/10.1007/978-981-10-7605-3_194

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