Risk monitoring method and system for quality supervision of clinical trial research center

A technology of clinical trials and research centers, applied in the field of clinical trial research, can solve the problems of untimely acquisition, inaccurate data, and large manpower, and achieve the effects of high automation, high reliability, timely and accurate quality supervision and risk monitoring

Pending Publication Date: 2020-04-28
上海太美星云数字科技有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0006] The calculation method of the above risk indicators requires the collection and calculation of massive data, which requires a huge amount of manpower, and there are problems such as inaccurate and untimely acquisition of data

Method used

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  • Risk monitoring method and system for quality supervision of clinical trial research center
  • Risk monitoring method and system for quality supervision of clinical trial research center
  • Risk monitoring method and system for quality supervision of clinical trial research center

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Embodiment Construction

[0032] In order to make the above objects, features and advantages of the present invention more comprehensible, specific implementations of the present invention will be described in detail below in conjunction with the accompanying drawings.

[0033] In the following description, many specific details are set forth in order to fully understand the present invention, but the present invention can also be implemented in other ways than those described here, so the present invention is not limited by the specific embodiments disclosed below.

[0034] As indicated in this application and claims, the terms "a", "an", "an" and / or "the" do not refer to the singular and may include the plural unless the context clearly indicates an exception. Generally speaking, the terms "comprising" and "comprising" only suggest the inclusion of clearly identified steps and elements, and these steps and elements do not constitute an exclusive list, and the method or device may also contain other st...

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Abstract

The invention relates to a risk monitoring method and a system for quality supervision of a clinical trial research center, and the method comprises the following steps: providing an index configuration setting page, and receiving a first input of a normal value range and a weight of a risk index on the index configuration setting page; providing a docking configuration page, and selecting a clinical test research center to be subjected to quality supervision on the docking configuration page; acquiring data related to the risk indexes from the selected clinical test research center; calculating the risk index according to the data; dividing the risk indexes into a plurality of risk files according to the risk degree; and providing a result display page, simultaneously displaying a plurality of risk indexes of the plurality of clinical trial research centers on the result display page, and representing different risk files by using different colors. According to the method, quality supervision and risk monitoring can be timely and accurately carried out on a clinical test research center.

Description

technical field [0001] The invention mainly relates to the field of clinical trial research, in particular to a risk monitoring method and system for quality supervision of clinical trial research centers. Background technique [0002] The clinical trial research center is the main body that conducts clinical trial research. In order to ensure the smooth progress of clinical trial research, it is necessary to carry out quality supervision of each clinical trial research center, timely discover risk factors and take corresponding intervention measures. The tools currently used to manage clinical trial data include clinical trial management system (CTMS, Clinical Trial Management System), clinical trial electronic document management system (eTMF, Electronic Trial MasterFile) and clinical trial electronic collection system (EDC, Electronic Data Capture), etc. These tools can help researchers manage the processes, documents, and data of clinical trial research. However, there...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G06Q10/06
CPCG06Q10/0635
Inventor 段成辉
Owner 上海太美星云数字科技有限公司
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