Skip to main content

A Risk Driven Approach to testing Medical Device Software

  • Conference paper
  • First Online:
Advances in Systems Safety

Abstract

Software for medical devices is strongly driven by regulatory requirements. Among those, safety assurance is critical. To achieve the required high levels of safety, it is essential to reliably reduce safety risks to a residual low level. This requirement is verified and validated mostly with software testing. An approach to software testing driven by safety risks is presented and complemented with comments from a real project where it has been applied. Specific comments to improve test design so as to detect more safety risks and issues are also provided based on experiences from the same project.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • AAMI (1993) AAMI HE48:1993 Human factors engineering guidelines and preferred practices for the design of medical devices. Association for the Advancement of Medical Instrumentation

    Google Scholar 

  • AAMI (2001) AAMI SW68:2001 Medical device software – software life cycle processes. Association for the Advancement of Medical Instrumentation

    Google Scholar 

  • AAMI (2004) AAMI TIR32:2004 Medical device software risk management. Association for the Advancement of Medical Instrumentation

    Google Scholar 

  • Copeland L (2003) A practitioner’s guide to software test design. Artech House Publishers, Boston and London

    Google Scholar 

  • Dustin E, Rashka J, Paul J (1999) Automated software testing: introduction, management and performance. Addison Wesley

    Google Scholar 

  • EC (1993) 93/42/EEC European Council directive concerning medical devices

    Google Scholar 

  • EC (1998) 98/79/EC European Parliament and Council directive on in vitro medical devices

    Google Scholar 

  • FDA (1996) 21 CFR Part 820 Quality system regulation. US Food and Drug Administration

    Google Scholar 

  • Fewster M, Graham D (1999) Software test automation. ACM Press/Addison-Wesley

    Google Scholar 

  • Graham D, van Veenendaal E, Evans I, Black R (2007) Foundations of software testing. Thomson Learning, London

    Google Scholar 

  • ISO (2000) ISO 14971:2000 Medical devices – application of risk management to medical devices

    Google Scholar 

  • Nielsen J (1993) Usability engineering. Morgan Kaufmann, San Francisco

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2011 Springer-Verlag London Limited

About this paper

Cite this paper

Benet, A.F. (2011). A Risk Driven Approach to testing Medical Device Software. In: Dale, C., Anderson, T. (eds) Advances in Systems Safety. Springer, London. https://doi.org/10.1007/978-0-85729-133-2_10

Download citation

  • DOI: https://doi.org/10.1007/978-0-85729-133-2_10

  • Published:

  • Publisher Name: Springer, London

  • Print ISBN: 978-0-85729-132-5

  • Online ISBN: 978-0-85729-133-2

  • eBook Packages: Computer ScienceComputer Science (R0)

Publish with us

Policies and ethics