Biennial inventory
A complete physical inventory of all controlled substances on hand at least once every two years, with a written record maintained for at least two years — drafted and reconciled against purchase and dispensing records.
VetLedger assembles a documentation-complete controlled-substance reconciliation and audit-readiness pack — every purchase record reconciled, every dispensing log verified, the biennial inventory drafted, and, when a theft or loss occurs, the DEA Form 106 and one-business-day notification — checked against federal and state recordkeeping requirements before a licensed pharmacist or former DEA diversion investigator certifies it.
A veterinary practice's DEA compliance is only as strong as its reconciliation. Miss a purchase invoice, misrecord an administration, skip the biennial inventory, or fail to report a theft within one business day — and the practice faces civil penalties that routinely exceed $1 million in aggregate.
In August 2025, a federal court entered a $956,709 default judgment against a veterinarian who could not account for 9,796 dosage units of oxycodone and hydrocodone. The average practice has 11 potential DEA infractions at any given time, according to a named compliance firm's survey.
Most practices run this by hand, from memory, once or twice a year. The regulations have not been read end-to-end since the last audit. That is exactly where compliance gaps hide.
VetLedger 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 21 CFR 1304.11, 1301.76(b), and related DEA recordkeeping requirements. These are the provisions each pack is held to.
A complete physical inventory of all controlled substances on hand at least once every two years, with a written record maintained for at least two years — drafted and reconciled against purchase and dispensing records.
Notification to the DEA within one business day of discovering a theft or significant loss, followed by a complete DEA Form 106 within 45 calendar days — drafted and timed to the federal clock.
Complete and accurate records of receipt, administration, dispensing, and disposal of controlled substances, reconciled against distributor invoices and physical counts.
The inventory must include the name, dosage form, strength, and quantity of each controlled substance, verified against DEA Schedule classification.
All records must be maintained for at least two years and be readily available for inspection — the pack includes a recordkeeping checklist and retention schedule.
Records of disposal of controlled substances, including the method and date, reconciled against reverse distributor documentation and witness signatures.
AI extracts and drafts. Deterministic rules — running as code, outside the model — decide what is complete. A licensed pharmacist or former DEA diversion investigator certifies every release. That order is never reversed.
Upload purchase invoices, dispensing logs, and physical count records. We return a free completeness read: which regulatory elements and reconciliations you already have, and which are missing.
As your authorized clerical agent, we ingest distributor invoices (Covetrus, MWI, Patterson, Henry Schein), administration/dispensing logs, and physical inventory sheets, and build a reconciled expected-balance ledger per drug and DEA schedule.
The biennial inventory report, audit-readiness narrative, and — if triggered — the DEA Form 106 and one-business-day notification are drafted from your validated data and the CFR rule pack into field-locked templates — no legal opinions, no invented facts.
Purchase records reconcile to dispensing logs to the dosage unit; the biennial inventory date is verified; the theft/loss notification clock is computed; any discrepancy above materiality threshold blocks release.
A licensed pharmacist or former DEA diversion investigator reviews the exception queue and certifies the pack. High-value or complex cases route to senior review.
You receive the pack: reconciled ledger, biennial inventory report, audit-readiness checklist, DEA Form 106 (if applicable), notification draft, and a compliance calendar — ready for the practice to submit under its own name.
The deliverable is completeness itself — every regulatory element and reconciliation 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 reconciliations as your clerical agent. We never provide legal advice, practice veterinary medicine, or interact with the DEA on your behalf.
Simple, predictable, and aligned with a documentation standard — not an open-ended consulting engagement.
Start with a free Compliance Gap Scan. Send your purchase invoices, dispensing logs, and physical count records and we'll return a completeness read against every subsection of 21 CFR 1304.11 and 1301.76(b).
Documentation-completeness service · not legal advice · the practice submits every report.