Safety Surveillance for Ongoing Clinical Trials

ClinicalBase Trial is a flexible and highly efficient surveillance tool designed to assist in the monitoring of safety in ongoing clinical trials.

This web-based solution allows you to define Clinical Research Forms, so it can be used independently of external clinical databases in small-scale clinical trials. ClinicalBase Trial includes a complete patient and laboratory database with visit plans and lab data for use in Integrated Patient and Clinical Trial surveillance.

The clinical trail data in ClinicalBase Trial is fully integrated with serious adverse event information and reporting in SafetyBase Interchange. With the statistics tool, the user can view advanced graphic displays, including crucial information about the correlation between lab data, drugs, and adverse event registrations.

It features high-speed Adverse Event entry and data transfer from electronic data capture. Data is uploaded through automatic import and verification tools.

Access is simple and flexible with a convenient and user-friendly web-based interface.

ClinicalBase Trial is fully compliant with present legislation and standards. Moreover, data can be automatically exported to other IT solutions, such as Oracle Clinical, through BaseCon’s Open Standard systems.

Key Features:

• Ongoing Real-Time Safety Monitoring.
• Clinical Trial Data and Adverse Events Integration.
• Define Clinical Research Forms.
• Advanced Statistics: Displays & Reports.
• Visit Plans & Patient Information Overviews.
• Online High-Speed Transfer & Upload of Data.
• Automatic Lab Data Import & Verification.
• Trial Visit plans, Patient Information & Lab Data.
• Graphic Patient Benchmarking Displays.
• Web-based and Flexible.

View the ClinicalBase Trial in action. Click here to view an animated demo