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by exact.works
Review drug labeling against FDA requirements including PLR format, content requirements, and consistency with approved package insert.
Real-time due diligence session. Upload target documents, conduct structured Q&A, receive a formatted memo with findings and flagged risks.
Three-agent pipeline that ingests multiple documents, cross-references them for conflicts and gaps, and produces a unified synthesis report with executive summary.
Accepts raw data and prepares structured regulatory filing drafts with required fields populated and human-review flags clearly marked.