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Overview

MedDRA (the Medical Dictionary for Regulatory Activities) is used to report adverse event data from clinical trials using standard terminology. We use the CTCAE (Common Terminology Criteria for Adverse Events) which in term can be mapped to the corresponding MedDRA code.

How it Works

Import the variable group into your StudyTRAX project in the Encounter Variables section:  Adverse Event (CTCAE mapping to MedDRA).xml

  • When a CTCAE (Common Terminology Criteria for Adverse Events) Term is selected from the pick-list, the corresponding MedDRA term and code are automatically populated.
  • Assign the variable group to a non-fixed Adverse Event interval

More Information on CTCAE

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