Every COA you check becomes a logged lot. Veritura reads the documentation, scores it against live FDA enforcement and recall records, and clears it. From a cleared lot you issue a verifiable Evidence Passport on every order, from your dashboard or the API. If a supplier is later hit by an FDA enforcement or recall signal, every lot and every passport you issued already knows, and so does the clinic that received it. One system of record across your whole supply chain. We verify the paperwork, never the product.
The platform
Every COA you check becomes a logged lot, the system of record for your supply. From there: score a document's risk, qualify and watch a supplier, issue a verifiable Evidence Passport on every order from your dashboard or the API, and pull a board-ready inspection packet in one click. Every capability is independent of the supplier, works across every vendor you use, and ends in the same defensible, verifiable record.
Paste any COA or supplier page, any supplier, no account, no network to join. Surfaces first-pass gaps and reuse signals on the spot, then routes serious cases into a reviewed audit.
✓ Open to any supplier, independent & free
Run a check →A human-reviewed memo on COAs, lab reports, supplier claims, source files, hashes, gaps, and memo-safe follow-up questions, run it before you commit to a supplier, not after.
✓ Pre-purchase diligence, independent of the seller
See pricing →Checks the supplier's claimed API source against FDA-source evidence, registration, DMF/LOA, NDC, cGMP, and oversight posture. We verify the source signal; we don't just reprint it.
✓ We check the source, not just display it
See intelligence →Run a supplier's packet and get a persistent, per-supplier readiness record, ready, gaps to close, or hold, with exactly what evidence is missing before you operationally trust them.
✓ Buyer-side qualification, a supplier portal can't tell you this
Qualify a supplier →A controlled dashboard for packet routing, memo QA, status tracking, PDF delivery, and account history, plus your own verifiable proof links to hand customers.
✓ Your own trust layer, not a supplier's network
Partner program →Issue a verifiable proof on every order from a cleared lot, tying it to its exact lot, COA, supplier, and reviewer, with a customer-safe verify link or QR. Dashboard one-click or POST /v1/passports at $3 each. The passport stays bound to its lot, so a later FDA recall reaches it, and the clinic that received it.
✓ Independent, verifiable, recall-aware proof on every order
Explore the passport →We keep your saved suppliers and lots on a recurring FDA enforcement and recall watch, then alert when a new strong source or lot match needs review.
✓ Recurring monitoring across saved suppliers and lots
Start watching →When an FDA or board records request lands, one click assembles your lots, suppliers, the diligence you performed, every issued passport, and any FDA recall exposure into one organized, inspector-ready PDF.
✓ A one-business-day records request, answered in a click
See the packet →Build Veritura into your own checkout: call one endpoint at order time and get a clear, review, or hold decision on the documentation and public records behind the order.
✓ Independent verification, right in your order flow
Talk to us →Who it's for
For busy clinics, prescribers & telehealth
You don't need to be a documentation expert. Paste a COA, get a clear verdict and the one thing to do next, and show your patients you check the paperwork on every batch.
Paste or upload any peptide or compounded-medication COA and get an independent read in seconds. No expertise, no setup, no overhead.
A clear documentation-risk score and one recommended next step, so a busy prescriber knows exactly what to act on, not a wall of jargon.
Hand patients a tamper-evident verification link showing the paperwork behind their lot was independently checked. We verify the paperwork, never the product.
The intelligence
Because Veritura sees across every vendor and checks against live FDA data, it surfaces what no single packet review can. Veritura checks the paperwork behind the paperwork: what is present, what conflicts, What is missing, and what needs human review before reliance. See the full intelligence →
The same lot, report ID, file, or available visual fingerprint appearing across indexed records, surfaced as a review signal.
Signature or stamp-region reuse is flagged when visual fingerprints are available and comparable.
ForensicsCOAs last touched by Word or a PDF editor, not a LIMS.
Producer anomalyLots and firms checked live against openFDA enforcement.
Reality checkVerification links that don't resolve or match the lot.
Live link checkFree 60-second self-check · no signup
Answer six questions and get an exposure score, plus exactly where the gaps are and what an independent record fixes. Nothing is stored unless you ask.
The deliverable
Not a score in a dashboard you forget, a defensible, exportable evidence record built for a board, a buyer, or an FDA inspector.
Why it matters
| Capability | Manual review | Veritura |
|---|---|---|
| Cross-vendor reuse detection | ✕ | ✓ |
| Live FDA enforcement / recall check | manual lookup | ✓ automatic |
| Document forgery & tamper signals | ✕ | ✓ |
| Scanned-COA OCR | retype by hand | ✓ |
| Hashed, reconstructable evidence trail | ✕ | ✓ |
| Continuous re-checking & alerts | ✕ | ✓ |
| Customer-safe proof record | ✕ | ✓ |
| Time per packet | hours | minutes |
Flagship product
When a customer, a board, or a state inspector asks for the exact COA, lot, and supplier packet behind one specific order, Evidence Passport produces it instantly, with a customer-safe view you can share.
Request a pilotUse cases
Catch a reused, altered, or unregistered-source COA before a lot is ever compounded, and keep the evidence on file.
Reconstruct any lot's documentation in seconds and keep your supplier-evidence trail defensible under FDA scrutiny.
Tie each order to its lot, COA, and reviewer, recall-ready and dispute-ready, with a proof view customers can see.
Route packets through one private workspace with memo QA, status, and delivery, a diligence benefit your members can't get alone.
How it works
No setup, no configuration. Send a document; get an answer you can act on and show your board. See the full process →
The reused-signature catch alone would have taken our team days of manual cross-checking, and we'd probably have missed it. This is the layer compounding has needed.
FAQ
As the FDA tightens enforcement, the supplier-evidence trail is the first thing re-examined. Make yours defensible before someone asks.