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MedDRA (the Medical Dictionary for Regulatory Activities) is used to report adverse event data from clinical trials using standard terminology. We use the The CTCAE (Common Terminology Criteria for Adverse Events) which in term can be mapped to the corresponding MedDRA codecorresponding MedDRA term and code.
How it Works
Import the variable group into your StudyTRAX project in the Encounter Variables section: Adverse Event (CTCAE mapping to MedDRA).xml
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