tooluniverse-clinical-data-integration
End-to-end drug safety review integrating FDA labels, FAERS adverse event reports, PRR/ROR disproportionality, pharmacogenomic biomarkers, clinical trial data, and published literature. Use for regulatory drug safety reviews, comprehensive pharmacovigilance reports, label-vs-real-world AE comparison, and clinical decision support for drug safety.
The canonical home for this skill is tooluniverse-clinical-data-integration in mims-harvard/ToolUniverse
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