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Assessing the Quality and Performance of Human Research Protection Programs to Guide Compliance Oversight Activities

机译:评估人类研究保护计划的质量和表现,以指导合规性监督活动

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摘要

Routine on-site reviews should focus primarily on facilities that are at risk of harming human subjects. Using human research protection program performance metric data from 107 facilities, we defined a facility to be at risk when one of its noncompliance/incident rates was among the top three highest rates of that performance metric. Based on 14 performance metrics with noncompliance and incidents in 2017, 27 facilities were identified to be at risk. These 27 facilities at risk, while constituting only 25% of all facilities, contributed to 70% +/- 25% (M +/- SD; range = 32%-100%) of all reported noncompliance/incidents. Thus, performance metric data can be used to guide compliance oversight activities.
机译:常规现场评论应主要关注有可能损害人类受试者的设施。 使用来自107个设施的人力研究保护计划性能度量数据,我们将其定义了一个有风险的设施,因为其一个不合规/事件率是该绩效指标的前三名最高率之一。 根据2017年的非融合和事件的14个绩效指标,确定了27种设施面临风险。 这27个危险的设施,同时仅构成所有设施的25%,贡献了所有报告的非融合/事件的70%+/- 25%(+/- SD;范围= 32%-100%)。 因此,性能度量数据可用于指导合规性监督活动。

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