Report management
A clinical trial is a sensitive process where all data and actions must be tracked and accounted for. Thus, all the eClinical products have a comprehensive reports database for you to find and track needed information.
In CTMS, to track and maintain the main processes of the application, you can find the following group of reports:
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Study Quality Control: analyze comprehensive data on protocol deviation cases and monitoring tasks completion organized by study, country or region, and site.
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Investigational Product: get investigational product statistics, such as therapeutic fields to which the drug belongs, studies in which it is involved, and so on.
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On-Demand Report: compile the custom-generated comprehensive reports on monitoring visits and letters and site basic information.
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Exceptional Handling: reassign the tasks of inactive users or approvers to active ones.
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Operation History: analyze changes over time, such as the name of the operation and operator, the time when the operation took place, and any additional comments to support the operation executed on the business categories or their related activities.
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Log Management: analyze the log of all the user actions within the CTMS applications, their details, and when they occurred.
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Job: set up system-executed data extraction jobs to get specific reports on a schedule and put them on the preset server where interested parties can access them.
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Audit Trail: analyze the comprehensive log of records associated with the actions performed on the business categories in CTMS, such as protocol deviation, trip report, ICF Tracking Log, and so on.
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Change History: analyze the complete history of changes made to instances, for instance, trip reports, of certain business categories in a study.