Drug test data control method and system

A technology of test data and control methods, applied in the information field, can solve problems such as missed inspection, re-inspection or wrong inspection, shortened test cycle, and wrong test data, so as to achieve the effect of improving quality and effectiveness, and improving combing and storage efficiency

Pending Publication Date: 2021-09-28
BEIJING ANZHEN HOSPITAL AFFILIATED TO CAPITAL MEDICAL UNIV
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Problems solved by technology

[0003] In the actual implementation of various hospitals and scientific research institutes, drug test data are often processed by manual recording and manual screening, and then simple data recording and storage are performed through a simple data information system for basic data aggregation and processing. , often lead to errors in experimental data due to the uncertain factors brought about by the work
[0004] And during this period, manual screening of existing data and problem monitoring are prone to errors, and it is impossible to effectively monitor the quality of a large

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  • Drug test data control method and system
  • Drug test data control method and system

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Embodiment Construction

[0051] Embodiments of the present invention will be described in detail below in conjunction with the accompanying drawings. It should be clear that the described embodiments are only some of the embodiments of the present invention, but not all of them. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without creative efforts fall within the protection scope of the present invention.

[0052] Those skilled in the art should know that the following specific embodiments or specific implementation methods are a series of optimized configurations listed by the present invention to further explain the specific content of the invention, and these configurations can be combined with each other or used in association with each other, unless it is clearly stated in the present invention that some or a specific embodiment or implementation cannot be associated with or used in conjunction with other embodiments or ...

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Abstract

The invention discloses a drug test data control method and system, and the system comprises: a quality control link processing module which is used for inputting control template data based on a quality control point of a drug clinical test; a data verification center module which is used for receiving the control template data of the quality control link processing module and converting non-standard data in the control template data into uniform structural data; a project center module which is used for summarizing clinical test project information and serves as a unified output port of the clinical test project information; a data storage center module which is used for storing effective data in clinical test items; and a system auditing module which is used for performing calculation based on the effective data of the clinical test project to obtain a project quality control content item. According to the scheme, full-process monitoring and processing of the drug test data are achieved, the error rate in the processes of data recording, screening and the like is effectively reduced, the carding and storage efficiency of the data is greatly improved, and the quality and effectiveness of basic data are improved.

Description

technical field [0001] This solution belongs to the field of information technology, and is mainly aimed at the control and processing of massive data in trials, especially for the control and processing of various types of drug trials and clinical effect data. Background technique [0002] Before the drug properties and large-scale clinical use of drugs, a large number of drug trials are generally required to effectively judge and sort out the specific properties and effects of different drugs. Clinical trial data is the basis for evaluating the results of clinical trials of drugs. The correctness, standardization, and effectiveness of data processing are extremely important, and generally require reliable traceability. In the field of pharmacology, drug test data generally have a long acquisition cycle and a huge amount of data, and processing and quality analysis are a huge workload. [0003] In the actual implementation of various hospitals and scientific research insti...

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Application Information

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IPC IPC(8): G16H70/40
CPCG16H70/40
Inventor 林阳仇琪赵桂平李妍周黎黎
Owner BEIJING ANZHEN HOSPITAL AFFILIATED TO CAPITAL MEDICAL UNIV
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