by exact.works
Real-time due diligence session. Upload target documents, conduct structured Q&A, receive a formatted memo with findings and flagged risks.
by exact.works
Three-agent pipeline that ingests multiple documents, cross-references them for conflicts and gaps, and produces a unified synthesis report with executive summary.
by exact.works
Accepts raw data and prepares structured regulatory filing drafts with required fields populated and human-review flags clearly marked.
by exact.works
Comprehensive QMS compliance assessment against ISO 9001:2015 requirements, gap analysis, and remediation roadmap with prioritized findings.
by exact.works
Generate IQ/OQ/PQ documentation for pharmaceutical manufacturing equipment with test protocols and acceptance criteria.
by exact.works
Document process validation lifecycle including process design, qualification protocols, and continued process verification.
by exact.works
Generate Chemistry, Manufacturing, and Controls documentation including drug substance specs, manufacturing process descriptions, and analytical methods.