Every regulated document,
written like a regulator.

X3 SOP is the AI Regulatory Document Intelligence Platform. It builds any regulated document — a one-page SOP to a 500-page manual — through a publishing house of AI specialists, grounded in the real CFR, and stores every clause as a living, connected object.

Grounded in 49 CFR · 40 CFR · 29 CFR · FMCSA / OSHA / EPA / PHMSA conventions — not an imitation of any author

X3 Author™ — a publishing house, not one AI

No single model writes your document. A composite author of specialists each owns one job, and the Executive Publisher makes it read as one seasoned voice — authoritative like a regulator, clear enough for a new employee to follow.

Executive Publisher

Owns voice, tone, structure, continuity. Nothing publishes without approval.

Chief Technical Author

Publication-quality SOPs, policies and manuals in the X3 house style.

DOT Regulatory Scholar

FMCSA, 49 CFR, guidance and enforcement — responsible for accuracy.

Citation Specialist

Every CFR citation and definition verified; stale rules flagged.

Documentation Architect

Hierarchy, sections, cross-references, appendices, numbering.

Compliance Validator

Required sections, records, training, notices and retention.

Risk Engineer

Liability, ambiguity, conflicts and insurance exposure.

Plain-Language Specialist

Regulation turned into language a real person can follow.

…and a growing staff: Instructional Designer, Legal Editor, Technical Illustrator, Version Historian, Translation, and more.

The publishing pipeline is the moat

Every document runs the same disciplined path — the reason the output reads like a Fortune 100 compliance department, not a chatbot.
1

Research & architect

The Documentation Architect designs the outline; the DOT Scholar maps each section to its governing regulation.

2

Author & cite

The Technical Author writes in the X3 house style; the Citation Specialist grounds every requirement in the real, current CFR.

3

Validate & publish

Compliance and readability are checked, a health score assigned, and the document exports to Word or PDF — stored as clauses.

The Clause Genome & Regulatory Knowledge Graph

We don't store files. We store thousands of intelligent clauses — each knowing its regulation, purpose, risk, and plain‑language meaning.
"What's affected if FMCSA updates Part 382?"
X3 SOP instantly traces every clause and document that depends on it — Drug & Alcohol Policy, Supervisor Training, Driver Handbook, Return-to-Duty, Clearinghouse Procedure, Audit Checklist — then (Phase 2) drafts the revisions and routes them for approval.
SOPsPoliciesTraining manualsForms & checklistsAudit responses
That turns X3 SOP from a writer into a regulatory knowledge operating system for the whole X3 ecosystem.

Pricing

Sell outcomes, not documents. 7‑day free trial on every plan.
Starter
$79/mo
  • Personal library
  • Core AI generation
  • Standard templates
  • Version history
Start free
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Professional
$199/mo
  • Unlimited documents
  • Full AI review team
  • Clause genome + export
  • Collaboration
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Business
$499/mo
  • Org-wide library
  • Approval workflows
  • Clause library
  • Regulatory impact analysis
Start free
Enterprise
$999+/mo
  • Custom knowledge base
  • White-label + API + SSO
  • Enterprise search
  • Multi-company
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X3 SOP is an educational compliance drafting aid, not legal advice. Every document is grounded in the CFR and marks unknown facts as [CONFIRM]; review and verify against the current regulations before adopting. Part of the X3 family: X3 Verify audits what X3 SOP writes.