Methods and systems for clinical trial data management
    1.
    发明授权
    Methods and systems for clinical trial data management 有权
    临床试验数据管理方法与系统

    公开(公告)号:US07783072B2

    公开(公告)日:2010-08-24

    申请号:US11380626

    申请日:2006-04-27

    IPC分类号: G06K9/00

    CPC分类号: G06Q10/10 G06F19/00 G16H10/20

    摘要: The invention provides systems and methods for creating certified copies of original information, including original hardcopy documents, in compliance with federal regulations and guidelines. The present invention also provides systems and methods of data management, and in particular, management of such certified copies. In some embodiments the invention relates to original clinical trial information such as source documents, and methods and systems for creating certified copies of such information to create an accessible central repository of such certified copies.

    摘要翻译: 本发明提供了根据联邦法规和指南,创建原始信息的认证副本(包括原始硬拷贝文件)的系统和方法。 本发明还提供数据管理的系统和方法,特别是管理这种认证副本。 在一些实施方案中,本发明涉及原始临床试验信息,例如源文件,以及用于创建这种信息的认证副本的方法和系统,以创建这种认证副本的可访问中央存储库。

    Methods and Systems for Clinical Trial Data Management
    2.
    发明申请
    Methods and Systems for Clinical Trial Data Management 有权
    临床试验数据管理方法与系统

    公开(公告)号:US20060259783A1

    公开(公告)日:2006-11-16

    申请号:US11380626

    申请日:2006-04-27

    IPC分类号: G06F12/14

    CPC分类号: G06Q10/10 G06F19/00 G16H10/20

    摘要: The invention provides systems and methods for creating certified copies of original information, including original hardcopy documents, in compliance with federal regulations and guidelines. The present invention also provides systems and methods of data management, and in particular, management of such certified copies. In some embodiments the invention relates to original clinical trial information such as source documents, and methods and systems for creating certified copies of such information to create an accessible central repository of such certified copies.

    摘要翻译: 本发明提供了根据联邦法规和指南,创建原始信息的认证副本(包括原始硬拷贝文件)的系统和方法。 本发明还提供数据管理的系统和方法,特别是管理这种认证副本。 在一些实施方案中,本发明涉及原始临床试验信息,例如源文件,以及用于创建这种信息的认证副本的方法和系统,以创建这种认证副本的可访问中央存储库。