一个增强的敏捷V模型:符合监管机构的要求和从模型采用到医疗器械开发的经验
Aliya A Khan1, Muhammad U Akram1, Wasi H Butt1
1Department of Computer & Software Engineering, National University of Sciences and Technology, Islamabad, Pakistan.
Heliyon
|April 15, 2024
概括
本研究介绍了医疗器械开发的增强敏捷V模型 (EAV),集成敏捷和计划驱动的方法以满足监管标准. 该EAV模型确保了合规性,并提高了设备的安全性和效率.
科学领域:
- 医疗器械开发 医疗器械开发
- 医疗器械软件工程 医疗器械软件工程
- 医疗保健中的法规合规性
背景情况:
- 医疗器械开发集成硬件和软件,面临区域监管要求的挑战.
- 传统的计划驱动方法限制了软件的发展,而敏捷方法可能缺乏足够的规划和文档.
- 确保遵守指南和标准对于医疗企业至关重要.
研究的目的:
- 提出符合监管要求的医疗器械开发过程模型.
- 通过结合计划驱动和敏捷方法来增强现有的发展模式.
主要方法:
- 通过分析文献和麦克休的模型,开发了增强敏捷V模型 (EAV).
- 将EAV模型映射到MDEVSPICE框架中,以确保符合IEC62304标准.
- 通过波浪治疗医疗器械的案例研究来评估EAV模型.
主要成果:
- 该EAV模型支持敏捷和布式方法,促进需求适应和硬件软件集成.
- 该EAV模型完全符合MDEVSPICE和IEC62304标准.
- 统计分析和案例研究的实施显示了设备安全,效率和可用性 (P <0.05) 的显著改善.
结论:
- 拟议的EAV模型符合监管标准,并在开发波浪治疗装置时成功实施.
- 需要进一步的研究来确定该模型对更紧,更简单的医疗产品的适用性.
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