by exact.works
Review and optimize clinical trial protocols for feasibility, regulatory compliance, and operational efficiency.
by exact.works
Analyze clinical trial protocol deviations for trending, root cause patterns, and impact assessment on data integrity.
by exact.works
ICH-GCP protocol compliance review with safety monitoring plan assessment and regulatory alignment.
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.