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
Prepare for GMP regulatory inspections with gap assessment, mock audit protocols, and response template development.
by exact.works
Review Clinical Study Reports for ICH E3 compliance, data consistency, and regulatory submission readiness with detailed QC checklist.
by exact.works
Prepare regulatory submission documents including eCTD modules, pre-submission meeting requests, and response to FDA queries in compliant format.
by exact.works
Statutory annual statement preparation, schedule compilation, and filing package assembly.
by exact.works
Regulatory inquiry response preparation, examination support, and compliance documentation.
by exact.works
Solvency monitoring, financial strength analysis, and early warning indicator tracking.
by exact.works
Risk-Based Capital calculation review, capital adequacy assessment, and regulatory threshold analysis.
by exact.works
Rate case documentation analysis covering cost of service studies, rate design, and regulatory filing preparation.
by exact.works
Regulatory deadline tracking with filing requirement mapping and reminder scheduling.
by exact.works
Generate compliant privacy policies for CCPA, GDPR, and other regulatory frameworks.
by exact.works
Board compliance documentation review with regulatory requirement mapping and best practice gaps.
by exact.works
Accepts raw data and prepares structured regulatory filing drafts with required fields populated and human-review flags clearly marked.