Five OSP elements
Description of practices, recordkeeping system, list of substances, management practices, and plan for preventing commingling — all present, or the pack does not release.
The Compliance Engine assembles a submission-ready Organic System Plan, an audit-ready recordkeeping file, and SOE import-certificate handling — every regulatory element, every required record, the mock-inspection checklist, and the annual renewal calendar — checked against the letter of 7 CFR Part 205 before a specialist releases it.
A USDA-certified organic operation's annual inspection is only as strong as the OSP and records behind it. Miss one of the five required OSP elements, skip a required record, mis-time the renewal window, or fail to reconcile an input approval — and the inspection can result in a major noncompliance, suspension, or decertification.
Most operations run this by hand, from memory, once a year. The regulation has not been read end-to-end since the last time it mattered. That is exactly where completeness gaps hide.
The Compliance Engine exists to close that gap with a single, exhaustive standard applied identically to every file.
We do not summarize the law and hope. Every pack is scored against a versioned rule pack tied to the exact text of 7 CFR Part 205. These are the provisions each pack is held to.
Description of practices, recordkeeping system, list of substances, management practices, and plan for preventing commingling — all present, or the pack does not release.
Audit trail from seed to sale: production, harvest, handling, and sales records — reconciled and complete.
Every input screened against the National List of Allowed and Prohibited Substances; non-compliant inputs flagged.
For imported products, electronic import certificates in the Organic Integrity Database, with supply-chain traceability documentation.
Mock-inspection checklist, updated OSP, and evidence log — all sequenced on the calendar so nothing is missed.
Operation type (producer, handler, broker, importer) correctly identified; applicable requirements applied.
AI extracts and drafts. Deterministic rules — running as code, outside the model — decide what is complete. A human specialist signs every release. That order is never reversed.
Upload your operation details and current OSP (if any). We return a free completeness read: which regulatory elements and records you already have, and which are missing.
As your authorized clerical agent, we gather your production records, input receipts, supplier certificates, and import documentation, and build the audit trail.
The five OSP elements are drafted from your validated data and the 7 CFR Part 205 rule pack into field-locked templates — no legal opinions, no invented facts.
All required records are present; inputs are screened against the National List; the audit trail is reconciled; the mock-inspection checklist is resolved. Any failure blocks release.
An experienced organic-compliance specialist reviews the exception queue and signs the release. High-value or complex operations route to attorney review first.
You receive the pack: submission-ready OSP, audit-ready recordkeeping file, import certificates (if applicable), mock-inspection checklist, and the annual renewal calendar — ready for your certifier.
The deliverable is completeness itself — every regulatory element and record accounted for or explicitly exception-coded. Nothing is left implicit.
The gates that decide completeness are code, not a model's opinion. A drafting error cannot slip past a regulatory requirement.
We prepare documentation and run recordkeeping as your clerical agent. We never contact your certifier, give legal advice, or conduct the inspection.
Simple, predictable, and aligned with a documentation standard — not a cut of any certification outcome.
Start with a free Compliance Gap Scan. Send your operation details and current OSP (if any) and we'll return a completeness read against every subsection of 7 CFR Part 205.
Documentation-completeness service · not legal advice · the operation submits every document.