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Journal of Medical Engineering & Technology Volume 40, 2016 - Issue 3
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Innovation

An analytical approach to identifying potential use-related issues concerning a medical device under development

Suresh P. GuptaCambridge Consultants, Cambridge, UKCorrespondence[email protected]
&
Andy PidgeonCambridge Consultants, Cambridge, UK
Pages 61-71 | Received 23 Sep 2015, Accepted 13 Dec 2015, Published online: 21 Jan 2016

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Ronak Patel, Pravin Nair, Meenal Bhatnagar, Sridevi Khambhampaty & Suresh Gupta. (2022) Device Development for Biosimilars: Human Factor Engineering for a Teriparatide Pen. Expert Opinion on Biological Therapy 22:2, pages 331-343.
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Ronak Patel, Miten Mehta, Meghana Dahiya & Vinu Jose. (2021) A review of use errors reported in human factor validation studies of biological combination products. Journal of Medical Engineering & Technology 45:7, pages 582-592.
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R. Marshall Werner & Allison N. Soffa. (2023) Considerations for the development of a field-based medical device for the administration of adjunctive therapies for snakebite envenoming. Toxicon: X 20, pages 100169.
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Sylvia Pelayo, Romaric Marcilly & Tommaso Bellandi. (2021) Human factors engineering for medical devices: European regulation and current issues. International Journal for Quality in Health Care 33:Supplement_1, pages 31-36.
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Teodora Miclăuş, Vasiliki Valla, Angeliki Koukoura, Anne Ahlmann Nielsen, Benedicte Dahlerup, Georgios-Ioannis Tsianos & Efstathios Vassiliadis. (2019) Impact of Design on Medical Device Safety. Therapeutic Innovation & Regulatory Science 54:4, pages 839-849.
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