THE ULTIMATE SOLUTION FOR CLINICAL TRIAL ADVERSE EVENT REPORTING

Avicenna Clinical Trial Safety combines automation with a user-friendly interface, customized for any research protocol, to make adverse event recording and reporting fast and easy for investigators and study staff. Our platform

  • minimizes free text entry
  • employs auto-fills and dropdown menus
  • provides intelligent data enrichment

Avicenna Clinical Trial Safety can be deployed on computer or mobile devices, making it an ideal tool for studies that rely on trial participant to self-report side effects, symptoms, or any other adverse conditions that arise between study visits. Study coordinators are immediately alerted when participants log events, which can prompt immediate follow-up by the study team and intervention if necessary. Avicenna can be combined with other self-assessment tools to facilitate remote participation and minimize the need for frequent on-site visits.

Avicenna Clinical Trial Safety fully processes adverse drug events, providing study sponsors and investigators a data dashboard with read and edit capabilities. Our solution integrates with other safety databases and has full regulatory reporting functionality.

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