Live FDA enforcement + cross-vendor checks

Verify a supplier's documents before you rely on them.

Veritura checks COAs and supplier packets against the FDA's own records, and every document we've indexed, surfacing reused, altered, and unregistered-source signals a manual review can't catch. Document diligence only; signals are for human review, never approval or safety claims.

Run a free COA check Take the 60-second exposure check

Live FDA enforcement check Cross-vendor reuse detection SHA-256 evidence trail

PDF sample-semaglutide-coa.pdf

LIVE

1 Extracting fields (lot, lab, method)…

2 Cross-referencing 1,284 indexed COAs…

3 Checking FDA enforcement records…

4 Analyzing signature & document forensics…

Evidence reliability

Hold reliance, review required

Blocker Reused signature signal

This approval signature matches 2 other COAs from different suppliers.

sigmatchmatch

Attention Producer anomaly

COA was last edited in Microsoft Word, labs typically issue from a LIMS.

Blocker FDA enforcement match

Lot SMA-260422-A matched an open recall in openFDA enforcement data.

Attention Manufacturer not in FDA registration snapshot

No FEI / establishment match, request source-registration evidence.

Signals require human review. Veritura does not certify quality, approve suppliers, or make safety or FDA-approval claims.

Documents indexed

Reuse signals flagged

Labs verified

Live signal feed

Reused signature matched across 3 vendors · 2m ago COA edited in Word, not a LIMS · 14m ago Lot number reused on 2 unrelated packets · 31m ago Unregistered source flagged for review · 47m ago openFDA recall match on a submitted lot · 1h ago Dead verify link, QR didn’t resolve · 1h ago Reused signature matched across 3 vendors · 2m ago COA edited in Word, not a LIMS · 14m ago Lot number reused on 2 unrelated packets · 31m ago Unregistered source flagged for review · 47m ago openFDA recall match on a submitted lot · 1h ago Dead verify link, QR didn’t resolve · 1h ago

The platform

One independent evidence layer. Six ways in.

Start with a free public check, and grow into a full diligence workspace and order-level proof. Every path is independent of the supplier, works across every vendor you use, and ends in the same defensible, verifiable record.

Free · public

Public COA Check

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 →

Pre-purchase review

Supplier Packet Diligence

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 →

Reality check

FDA-Source Insight Check

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 →

Onboarding

Supplier Onboarding Readiness

Shows exactly what evidence is missing before a supplier should be operationally trusted, a clear, source-gap readiness picture for your shelf.

✓ Buyer-side readiness, a supplier portal can't tell you this

How it works →

For partners & teams

Private Partner Workspace

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 →

Flagship

Evidence Passport

Order-level proof tying each order to the exact lot, COA, supplier packet, reviewer, and customer-safe record, verifiable by link or QR, on any supplier.

✓ Independent, verifiable proof on any order

Explore the passport →

Who it's for

Built for the operators with COA, lot, and supplier exposure.

503A compounding pharmacies503B outsourcing facilitiesMed spas & wellness clinicsTelehealth fulfillment platformsGLP-1 / peptide infrastructureGPOs & buying groupsTesting & analytical labsProcurement & quality teams

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. See the full intelligence →

Cross-vendor reuse graph

The same signature, lot, or COA appearing across different suppliers, caught only because Veritura sees the whole index.

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

Free 60-second self-check · no signup

Not sure where your supplier paperwork stands?

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.

Check my exposure →

The deliverable

See exactly what you get.

Not a score in a dashboard you forget, a defensible, exportable evidence record built for a board, a buyer, or an FDA inspector.

Veritura · Supplier Diligence MemoVTR-SUP-20260606-7A41

Executive verdict

Hold reliance, request manufacturer identity evidence

Reused signature signal, matches 2 other COAs from different suppliers.

Producer anomaly, COA last edited in Microsoft Word, not a LIMS.

openFDA recall match, lot SMA-260422-A in open enforcement data.

Registration, no FEI / establishment match found.

Methodology v1.0SHA-256 a3f9…18c2

Executive verdict, the one decision, first.
Cited findings, every signal tied to evidence and a next step.
Evidence map + SHA-256, reconstructable at inspection time.
Supplier follow-up questions, copy-ready and memo-safe.
Reliability score you can track and improve over time.
Customer-safe Evidence Passport, shareable proof for your buyers.

Why it matters

What a manual review can't do.

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

Evidence Passport turns reviewed evidence into order-level proof.

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 pilot

1 Order & customer reference

2 Exact API / product & lot

3 COA & supplier packet (hashed)

4 Reviewer history & release state

5 Source gaps & reuse signals

6 Customer-safe proof record

Use cases

Built around how operators actually work.

503A pharmacy · Pharmacist-in-charge

Qualify a new API supplier with confidence

Catch a reused, altered, or unregistered-source COA before a lot is ever compounded, and keep the evidence on file.

503B facility · Director of Quality

Stay inspection-ready, every lot

Reconstruct any lot's documentation in seconds and keep your supplier-evidence trail defensible under FDA scrutiny.

Med spa / telehealth · Operations

Give every order customer-safe proof

Tie each order to its lot, COA, and reviewer, recall-ready and dispute-ready, with a proof view customers can see.

GPO / network · Partnerships

Offer members a trust layer

Route packets through one private workspace with memo QA, status, and delivery, a diligence benefit your members can't get alone.

How it works

One packet in. A defensible evidence record out.

No setup, no configuration. Send a document; get an answer you can act on and show your board. See the full process →

Supplier COAUploaded or emailed in

Veritura verifiesForensics · FDA · reuse

ForensicsFDAReuse

Evidence recordCited · hashed · shareable

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.

Director of Quality503B outsourcing facility · illustrative

Built with input from

PD PharmD & sterile-compounding advisors

RA Regulatory affairs & 503B quality leaders

FAQ

Questions, answered.

Do you certify quality or approve suppliers?

No. Veritura is document diligence only. We surface evidence signals for human review, we never certify product quality, approve a supplier, or make safety, legal, or FDA-approval claims.

What's actually in a report?

An executive verdict, a reliability posture, cited findings (with evidence IDs and SHA-256 hashes), an evidence map, memo-safe supplier follow-up questions, the methodology version, and a customer-safe Evidence Passport you can share.

How fast is it?

The free public check runs on screen in seconds. Human-reviewed paid memos are typically delivered within a couple of business days, depending on packet complexity.

Is my supplier data secure?

Documents and evidence records are encrypted in transit and at rest, with access scoped to your workspace. Practice and sample packets are isolated from billing and delivery.

Do you replace wet-lab testing?

No. We review the documentation and source evidence behind a supplier and API, we don't test product. We make the paper trail defensible; lab testing remains lab testing.

What does it cost?

503A/503B compounding pharmacies are free, they're how the network gets supplied. Clinics and prescribers pay $49 to $99/mo to check the paperwork, the Evidence Passport is $3 an order, and platforms are scoped to volume. See pricing.