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
Review cleaning validation documentation including residue limits, sampling strategies, and analytical method suitability.
by exact.works
Review and optimize clinical trial protocols for feasibility, regulatory compliance, and operational efficiency.
by exact.works
Review batch production records for GMP compliance, data integrity, and completeness with deviation flagging.
by exact.works
Review drug labeling against FDA requirements including PLR format, content requirements, and consistency with approved package insert.
by exact.works
Review Clinical Study Reports for ICH E3 compliance, data consistency, and regulatory submission readiness with detailed QC checklist.
by exact.works
Review MEP coordination models for clash detection issues and routing optimization opportunities.
by exact.works
Review construction documents against ICC building codes including IBC, IMC, IPC, and IECC.
by exact.works
Review construction contracts against AIA document standards, identify non-compliant clauses, and generate compliance recommendations.
by exact.works
ML underwriting fairness assessment, disparate impact analysis, and model documentation review.
by exact.works
Settlement practice analysis, payment timing review, and unfair claims practice detection.
by exact.works
TPA compliance review, service agreement validation, and performance monitoring.
by exact.works
Catastrophe model validation, exposure data quality review, and model output analysis.