Departmental Papers (CIS)

Date of this Version

June 2007

Document Type

Conference Paper

Comments

Postprint version. Presented at Joint Workshop on High Confidence Medical Devices, Software, and Systems and Medical Device Plug-and-Play Interoperability, June 2007.

Abstract

As software becomes ever more ubiquitous and complex in medical devices, it becomes increasingly important to assure that it performs safely and effectively. The critical nature of medical devices necessitates that the software used therein be reliable and free of errors. It becomes imperative, therefore, to have a conformance review process in place to ascertain the correctness of the software and to ensure that it meets all requirements and standards.

Formal methods have long been suggested as a means to design and develop medical device software. However, most manufacturers shy from using these techniques, citing them as too complex and time consuming. As a result, (potentially life-threatening) errors are often not discovered until a device is already on the market.

In this paper we present a safety model based approach to software conformance checking. Safety models enable the application of formal methods to software conformance checking, and provide a framework for rigorous testing. To illustrate the approach, we develop the safety model for a Generic Infusion Pump (GIP), and explain how it can be used to aid software conformance checking in a regulatory environment.

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Date Posted: 28 January 2008

This document has been peer reviewed.