Integrated Reporting

Sponsors and CROs want more robust reporting functionality from their EDC platform – without having to pay extra for it.  That’s why ClinicalAnalytics 4.0 uses innovative reporting technology that enables you to create either granular or more global reports of your data.   With drag and drop simplicity, ClinicalAnalytics 4.0 streamlines your ability to retrieve, isolate and audit data using configurable features that graphically display information for analysis.

Customers now no longer have to purchase additional third-party reporting tools.  Rather, with ClinicalAnalytics 4.0, they have advanced and powerful reporting tools that create, assess and validate data simply.  Configurable report functionality and an easy-to-use interface, meanwhile, enable rapid adoption across different users with different levels of technology sophistication.  From patient scheduling to aggregate reporting, ClinicalAnalytics 4.0 makes it easy for you to report on the progress and results of your study in real-time.

Integrated Reporting Features:

Browser Configurable Aggregated Study Reporting defines complex reports across multiple data sets, including audit trail information, and posts the results graphically in a variety of formats, such as Excel, SPSS and SAS.  Users can configure four kinds of reports:

  • Visit Reports – Shows how subject data has changed over the length of a study using graphical reporting to track data changes across different visits.
  • Summary Reports – Compares relationships between fields and/or subjects to data elements.
  • Data Listing – Allows the select extraction of selected subject form data with audit and data clarification form information.
  • Dictionary Coding – Pulls the results of coding progress to analyze and verify consistency.  In addition, users can just click the Coding link under Forms and view an activity task list, which provides an overview of ongoing and completed work.  This enables users to quickly assess the status of dictionary coding quickly.

Real-time Monitoring, Reporting and Validation automates patient and site-level reports, query generation, form completion, adverse events and Microsoft® Word documents using customizable dashboards. CA 4.0’s dashboards provide a snapshot on a study progress. Designers can configure and display different graphical charts in addition to illustrating summary data.

Study Metrics Report streamlines the management of your study in real-time by providing concise design and metrics reports.  From incremental data reports to DCF status, CA 4.0 offers 16 standard out of the box reports provided to summarize study data.

Patient Milestone Reporting creates a macro view of patient timelines to better manage scheduling and overall study performance.

Project Management freezes a project design to manage iterations and allow for controlled changes to be made on copies of the original design. As part of the protocol amendment work flow, project freeze ensures the continuity of projects, while optimizing the ability of users to make changes to copies that can be incorporated into the original design upon approval.

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