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Methods and systems for organizing, tracking, and using informed consent data for human specimen studies

机译:组织,跟踪和使用知情同意书数据进行人体标本研究的方法和系统

摘要

The subject matter described herein includes methods, systems, and computer program products for organizing, tracking, and using informed consent data for human specimen studies. According to one method, an informed consent document is organized and an agreement agreement is attached to the specimen. Consent terms and any changes to consent terms are tracked. Authorized use analysis of specimens and associated data is performed to provide a regulatory information knowledge base (RIK) that includes global regulatory data derived from private and public sources. The consent form is automatically generated using the consent document and RIK based on the structured information.
机译:本文描述的主题包括用于组织,跟踪和将知情同意数据用于人类标本研究的方法,系统和计算机程序产品。根据一种方法,组织知情同意文件,并在样本上附加协议协议。跟踪同意条款和对同意条款的任何更改。进行标本和相关数据的授权使用分析,以提供法规信息知识库(RIK),其中包括从私人和公共来源获得的全球法规数据。同意书是使用同意书和RIK根据结构化信息自动生成的。

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