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
Reviews FDA regulatory submissions for compliance. Covers 510(k), 21 CFR Part 11, and software as a medical device (SaMD) requirements.
by exact.works
Analyze bug bounty program performance, submission trends, and payout efficiency with optimization recommendations.
by exact.works
Performance rights compliance audit, venue licensing verification, and PRO reporting accuracy.
by exact.works
Music license compliance analysis, mechanical and sync license verification, PRO affiliation review.
by exact.works
Generate complete Production Part Approval Process documentation packages including all 18 elements for automotive supplier submissions.
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
Track and verify construction submittals against specification requirements and approval status.
by exact.works
Automated preparation of state Department of Insurance filings, form validation, and submission package assembly.
by exact.works
IRB submission compliance review with informed consent assessment and risk analysis.