How many testers are needed to assure the usability of medical devices?. (September 2014)

• Record Type: Journal Article
• Authors: Borsci, Simone; Macredie, Robert D; Martin, Jennifer L; Young, Terry
• Is Part Of: Expert review of medical devices. Volume 11:Number 5(2014)
• Page Start: 513
• Page End: 525
• Publication Date: 2014-09
• Subjects: Medical instruments and apparatus -- Periodicals; 610.28
• DOI: 10.1586/17434440.2014.940312
• Languages: English
• ISSNs: 1743-4440

Abstract

<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <p>Before releasing a product, manufacturers have to follow a regulatory framework and meet standards, producing reliable evidence that the device presents low levels of risk in use. There is, though, a gap between the needs of the manufacturers to conduct usability testing while managing their costs, and the requirements of authorities for representative evaluation data. A key issue here is the number of users that should complete this evaluation to provide confidence in a product's safety. This paper reviews the US FDA's indication that a sample composed of 15 participants per major group (or a minimum of 25 users) should be enough to identify 90–97% of the usability problems and argues that a more nuanced approach to determining sample size (which would also fit well with the FDA's own concerns) would be beneficial. The paper will show that there is no <italic>a priori</italic> cohort size that can guarantee a reliable assessment, a point stressed by the FDA in the appendices to its guidance, but that manufacturers can terminate the assessment when appropriate by using a specific approach – illustrated in this paper through a case study – called the 'Grounded Procedure'.</p> </abstract>