The intelligence

Findings a human reviewer can't produce.

Because Veritura sees across every vendor and checks against live FDA data, it surfaces what no single packet review can, reused signatures, recycled lots, documents edited outside a lab, and lots sitting in open enforcement. Signals for human review; we never call a document fake or make an approval or safety claim.

Cross-vendor reuse graph

The same signature, lot, or COA appearing across different suppliers, caught only because Veritura sees the whole index, not one packet at a time.

Reused signatures & stamps

The same signature pasted across COAs from different suppliers.

Forensics

Edited outside a lab

COAs last touched by Word or a PDF editor, not a LIMS.

Producer anomaly

Live FDA recall match

Lots and firms checked live against openFDA enforcement.

Reality check

Dead verify routes

Verification links that don't resolve or match the lot.

Live link check

Document forensics

A 13-signal pass on every document.

Presence or absence recorded mechanically, then reviewed by a human. See the methodology →

Signature reuse

Approval signatures matched across COAs from unrelated suppliers.

Forensics

Producer anomaly

Last-edited metadata showing Word or a PDF editor instead of a LIMS.

Producer anomaly

Lot & report reuse

Lot numbers and report IDs recycled across packets that shouldn't share them.

Forensics

Field completeness

Lot, lab, method, purity, MS/sequence, sterility, endotoxin, strength, and address presence.

Completeness

Method vs claim

Stated assay/method compared against the values and language actually present.

Reconciliation

Verification routes

Published verify links checked for whether they resolve and match the lot.

Live link check

Reality check

Checked against the FDA's own records.

Source-style evidence categories, captured with the search, source URL, and capture date preserved for the record.

openFDA enforcement & recalls

Lots and firms matched against open enforcement and recall data in real time.

Registration snapshot

Manufacturer identity, FEI / establishment, and registration posture, flagged when there's no match.

Source-chain gaps

DMF/LOA, NDC/listing relevance, and cGMP evidence categories tracked as rows, not as a verdict.

Why it matters

What a manual review can't do.

CapabilityManual reviewVeritura
Cross-vendor reuse detection
Live FDA enforcement / recall checkmanual lookup✓ automatic
Document forgery & tamper signals
Scanned-COA OCRretype by hand
Hashed, reconstructable evidence trail
Time per packethoursminutes

Run it on a real COA and see the signals.

Create a free workspace and check a document, or talk to us about your supplier base.