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  • Clinical Research Data Capture and Management System

    The system is designed based on foreign guidelines on CDM (clinical data management) such as GCDMP(Good clinical trial management practice) issued by Society for Clinical Data Management in the US, Writing Code Of Data Management Plan issued by European Clinical Research Data Management Association as well as regulations on GCP by ICH, WHO and China. It adopts state-of-the art data acquisition method-internet-based electronic data acquisition to construct multiple clinical research centers to conduct data management work in clinical research.

    Functions and Features

    Data acquisition

    Support various means of data acquisition, including manual data entry, direct capturing data from HIS, LIS, PACS and other systems, entry on mobile devices so as to satisfy capturing needs in different circumstances.

    Data check

    During the process of data entry, the system check the accuracy of all the data through comparison with normal value and effective value in addition to other means.

    Information exchange

    The system provides internet-based instant messaging function for timely exchange of messages between participants of the drug clinical trial and thus better data management.

    Information display

    The system provides the powerful statistic search engine that is able to meet varied statistic and search requirements by allowing users to custom combination of search conditions. It is also enable to display diversified search information for users to view search results more readily.

    System security

    The system has a perfect and secure ID authentication mechanism, ensuring the security of data and project documents. It adopts technologies of online data backup, online system update and online parameter maintenance, supporting a 7×24 non-stop operation.

    Data interface

    The system provides interfaces to specialized medical statistic software so that trial data can be directly exported to specialized medical statistic software for data analysis. Currently, the software supported by the interface are SAA and SPSS.

    Data verification

    The system provides SDV, manual check and logic verification as three genres of data verification. SDV targets electronic data that are inconsistent with paper data; manual check is conducted by the inspector on all electronic data; logic check is carried out automatically after relevant items to be checked are maintained into the system.

    System Platform

    Application Systems:

  • Server: IBM AIX、Windows 2003 Server、Windows 2008 Server
  • Client: Windows XP/ Vista/7/8
  • Database: DB2 and Oracle are recommended and it also supports other data bases
  • Middleware: IBM Websphere 7.0 or higher
  • Hospital Information Process Product Line
    Drug Clinical Trial Product Line
    Regional medical product line
    Hospital clinical information solutions
    Clinical Information Solutions for Outpatient
    Hospital Information Integration Solution
    Medical Technology Solution
    Clinical Research Solutions
    Drug Clinical Trial Management System
    Clinical Research Data Capture and Management System
    Ethical Review Management System
    Construction plans for regional EMR
    Electronic Personal Health Record
    The Centers for disease diagnosis and treatment solutions
    Collaborative Management Platform for Special Diseases