Taxonomy of surrogate users for the development and evaluation of medical devices from the end users’ perspective

Author:

Shah Syed Ghulam Sarwar,Robinson I.

Publisher

Springer Berlin Heidelberg

Reference27 articles.

1. Tsai W-T, Mojdehbakhsh R, Rayadurgam S. (1997) Experience in capturing requirements for safety-critical medical devices in an industrial environment. In: Proceedings of second IEEE High-Assurance Systems Engineering Workshop, 11–12 Aug 1997. Washington, DC.: pp 32–36.

2. Kaye RD. (2000) Human factors (HF) in medical device use safety: how to meet the new challenges. In: Proceedings of the XIVth Triennial Congress of the International Ergonomics Association and 44th Annual Meeting of the Human Factors and Ergonomics Association, ‘Ergonomics for the New Millennium’, July 29–August 4, 2000. San Diego, CA, United State. pp 550–552.

3. Shaw B. (1985) The role of the interaction between the user and the manufacturer in medical equipment industry. R&D Manage. 15: 283–292.

4. Biemans WG. (1991) User and third-party involvement in developing medical equipment innovations. Technovation 11: 163–182.

5. Shah SGS, Robinson I. (2006) User involvement in healthcare technology development and assessment: Structured literature review. Int. J. Health Care Qual. Assur., 19: (Accepted, in press).

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