Effectively Incorporating Human Factors into Ocular Device Development

Andrea M. Pisa, Natasha Fosker, Timothy Quigg
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Abstract

With the growing prevalence of metabolic disorders (Rupenthal, 2019) and the over-60s population set to increase from today’s 10% of the global population to over 20% in 2050 (Gaudana, Jwala, Boddu, & Mitra, 2009), incidence of ocular disease is rising (Royal College of Ophthalmologists, 2018). This is having a significant impact on the demand for ophthalmology care with a 30-40% increase predicted between 2018- 2038 (Royal College of Ophthalmologists, 2018). Together with leading pharmaceutical partners, Crux Product Design have worked on a range of cutting-edge ocular device development programs aimed to provide better outcomes for patients globally. This paper covers the novel approach to Human Factors applied within these programs, demonstrating the value added when going beyond the regulatory minimum and how successful incorporation of these methods starts with team culture, early and regular usability activities and the careful translation of insights into tangible design improvements.
有效地将人为因素纳入眼具开发
随着代谢紊乱的日益流行(Rupenthal, 2019)以及60岁以上人口将从今天占全球人口的10%增加到2050年的20%以上(Gaudana, Jwala, Boddu, & Mitra, 2009),眼部疾病的发病率正在上升(皇家眼科学院,2018)。这对眼科护理的需求产生了重大影响,预计在2018年至2038年之间将增长30-40%(皇家眼科学院,2018年)。与领先的制药合作伙伴一起,Crux产品设计致力于一系列尖端的眼科设备开发项目,旨在为全球患者提供更好的结果。本文涵盖了在这些程序中应用的人为因素的新方法,展示了当超出规定的最低限度时所增加的价值,以及如何成功地将这些方法与团队文化、早期和定期的可用性活动以及仔细地将见解转化为切实的设计改进相结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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