Innovation in Pediatric Medical Devices: Proceedings From The West Coast Consortium for Technology & Innovation in Pediatrics 2019 Annual Stakeholder Summit

Juan C Espinoza, Kathryn M. Cooper, Nadine Afari, P. Shah, S. Batchu, Y. Bar-Cohen
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引用次数: 4

Abstract

Pediatric medical devices cover a broad array of indications and risk profiles, and have helped to reduce disease burden and improve quality of life for numerous children. However, many of the devices used in pediatrics are not intended for or tested on children. Several barriers have been identified that pose difficulties in bringing pediatric medical devices to the market. These include a small market and small sample size; unique design considerations; regulatory complexities; lack of infrastructure for research, development, and evaluation; and low return on investment. In 2007, the Food and Drug Administration (FDA) created the Pediatric Device Consortia (PDC) Grants Program under the administration of the Office of Orphan Products Development. In 2018, the FDA awarded over US $30 million to five new PDCs. The West Coast Consortium for Technology & Innovation in Pediatrics (CTIP) is one of these PDCs and is centered at the Children’s Hospital Los Angeles. In February 2019, CTIP convened its primary stakeholders to discuss its priorities and activities for the new grant cycle. In this paper, we have presented a report of the summit proceedings to raise awareness and advocate for patients and pediatric medical device innovators as well as to inform the activities and priorities of other organizations and agencies engaged in pediatric medical device development.
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儿科医疗器械创新:西海岸儿科技术与创新联盟会议记录2019年度利益相关者峰会
儿科医疗设备涵盖了广泛的适应症和风险概况,并帮助减轻了许多儿童的疾病负担并提高了生活质量。然而,儿科中使用的许多设备并不是为儿童设计或对儿童进行测试的。已经确定了一些障碍,这些障碍给将儿科医疗设备推向市场带来了困难。这包括市场小、样本量小;独特的设计考虑;监管的复杂性;缺乏研究、开发和评估的基础设施;投资回报率低。2007年,美国食品和药物管理局(FDA)在孤儿产品开发办公室的管理下创建了儿科器械联盟(PDC)资助计划。2018年,FDA向5种新的PDCs拨款3000多万美元。西海岸儿科技术与创新联盟(CTIP)是这些PDCs之一,以洛杉矶儿童医院为中心。2019年2月,CTIP召集了主要利益相关者,讨论了新资助周期的优先事项和活动。在本文中,我们提交了一份首脑会议会议记录的报告,以提高对患者和儿科医疗器械创新者的认识和宣传,并告知从事儿科医疗器械开发的其他组织和机构的活动和优先事项。
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