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Tooluniverse Clinical Data Integration

Medical & Healthcare

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.

Publisher / source

mims-harvard/ToolUniverse (found on GitHub top repositories)

Upstream record

mims-harvard/ToolUniverse

Version

Version 1

Published

2026-11-11

Publication review

Approved for publication ยท recorded passed scan 2026-11-11

Content fingerprint

f884d55c4e4a03786091c59893efd8e300e175bcd706a9ae8cd7dd3f723aaeb5

Review before you use it

Publication approval is a recorded review state, not a guarantee of safe execution. Check the upstream license, required tools and permissions, and test in your intended client.

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Source: https://prompeteer.ai/skills-hub/c3367174-f86c-4211-9a72-e31c8fbdaae6