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    • 1. 发明申请
    • METHOD AND APPARATUS FOR ADMINISTERING CLINICAL TRIALS
    • 用于管理临床试验的方法和装置
    • US20150332022A9
    • 2015-11-19
    • US13081818
    • 2011-04-07
    • Zikria Qayoom SyedMatthew John WalzJeffrey Scott BurkChester Joseph Shemanski
    • Zikria Qayoom SyedMatthew John WalzJeffrey Scott BurkChester Joseph Shemanski
    • G06Q50/00G06Q10/00
    • G06F19/366G06F19/00G06Q10/06G06Q50/22G16H10/40
    • A system and method for administering a clinical trial centralizes all trial communications in a website system. The system enables a trial sponsor to create individual websites for each of its available trials using website templates driven by workflow management software. The prospective clinical investigator can browse current and upcoming clinical trials and select trials that he/she wants to participate in. The clinical investigator can register interest in the trial by entering their contact information and professional credentials to create a personal profile. The trial sponsor can search for prospective clinical investigators whose credentials are commensurate with those required for a clinical trial. The trial sponsor also can invite prospective clinical investigators to participate in clinical trials. The system programmatically creates a secure account the clinical investigator can use to access the clinical trial website (called a collaboration portal). Once the clinical investigator logs into the collaboration portal, he/she is able to appoint sub-investigators and additional administrative accounts for the portal. The clinical investigator also uploads essential trial documentation via the collaboration portal into the document repository that the trial sponsor set up for the clinical trial. The investigator portal also gives the principal investigator a central place to access clinical trial alerts, notifications and a to-do list.
    • 用于管理临床试验的系统和方法将所有试用通信集中在网站系统中。 该系统允许试用赞助商使用由工作流程管理软件驱动的网站模板为每个可用的试验创建单独的网站。 预期的临床研究者可以浏览当前和即将到来的临床试验,并选择他/她想参与的试验。临床研究者可以通过输入他们的联系信息和专业证书来注册试验,以创建个人资料。 试验赞助者可以搜索与临床试验所需资格相符的潜在临床研究者。 试验发起人还可以邀请临床研究人员参与临床试验。 该系统以编程方式创建一个安全帐户,临床研究人员可以使用它来访问临床试验网站(称为协作门户)。 一旦临床调查员登录到协作门户网站,他/她就可以为该门户指定副调查员和其他管理帐户。 临床研究者还将基本的试验文件通过协作门户上传到试验赞助商为临床试验设立的文件库中。 调查员门户还向主要调查员提供了访问临床试验警报,通知和待办事项列表的中心位置。
    • 2. 发明申请
    • METHOD AND APPARATUS FOR ADMINISTERING CLINICAL TRIALS
    • 用于管理临床试验的方法和装置
    • US20120259647A1
    • 2012-10-11
    • US13081818
    • 2011-04-07
    • Zikria Qayoom SyedMatthew John WalzJeffrey Scott BurkChester Joseph Shemanski
    • Zikria Qayoom SyedMatthew John WalzJeffrey Scott BurkChester Joseph Shemanski
    • G06Q50/00G06Q10/00
    • G06Q50/22G06Q10/06G16H10/40
    • A system and method for administering a clinical trial centralizes all trial communications in a website system. The system enables a trial sponsor to create individual websites for each of its available trials using website templates driven by workflow management software. The prospective clinical investigator can browse current and upcoming clinical trials and select trials that he/she wants to participate in. The clinical investigator can register interest in the trial by entering their contact information and professional credentials to create a personal profile. The trial sponsor can search for prospective clinical investigators whose credentials are commensurate with those required for a clinical trial. The trial sponsor also can invite prospective clinical investigators to participate in clinical trials. The system programmatically creates a secure account the clinical investigator can use to access the clinical trial website (called a collaboration portal). Once the clinical investigator logs into the collaboration portal, he/she is able to appoint sub-investigators and additional administrative accounts for the portal. The clinical investigator also uploads essential trial documentation via the collaboration portal into the document repository that the trial sponsor set up for the clinical trial. The investigator portal also gives the principal investigator a central place to access clinical trial alerts, notifications and a to-do list.
    • 用于管理临床试验的系统和方法将所有试用通信集中在网站系统中。 该系统允许试用赞助商使用由工作流程管理软件驱动的网站模板为每个可用的试验创建单独的网站。 预期的临床研究者可以浏览当前和即将到来的临床试验,并选择他/她想参与的试验。临床研究者可以通过输入他们的联系信息和专业证书来注册试验,以创建个人资料。 试验赞助者可以搜索与临床试验所需资格相符的潜在临床研究者。 试验发起人还可以邀请临床研究人员参与临床试验。 该系统以编程方式创建一个安全帐户,临床研究人员可以使用它来访问临床试验网站(称为协作门户)。 一旦临床调查员登录到协作门户网站,他/她就可以为该门户指定副调查员和其他管理帐户。 临床研究者还将基本的试验文件通过协作门户上传到试验赞助商为临床试验设立的文件库中。 调查员门户还向主要调查员提供了访问临床试验警报,通知和待办事项列表的中心位置。