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PlatformPlatform overviewDocument checksSupplier filesVeraCatoPassports and SealsClearGateCustodyIntakeAPIPricing
SolutionsCompounding pharmacies503B outsourcing facilitiesClinicsMed spasTelehealth platformsConsultantsSolutions overview
ResourcesMethodologyOrder-level COA traceabilitySupplier packet diligenceResource libraryPublic toolsIntelligenceTrust Center
CompanyAbout VerituraWhy independentPartnersFor counselContact
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Resources: Read how the check works before you rely on it.

Dated where true. Says where it stops.

Our method is published. Hold us to it.

Two standards, the release contract and the methodology are published for anyone to read. Each one says who it is for and where it stops.

Three documents define the work. Published, versioned and dated.

Each says what it requires, how the product meets it, and where it stops.

Orders in over the last 30 days at a sample pharmacy: 15, 5 matched on a packing slip, a week at a time, by how each came in: by API 6, from a watched folder 7, from the workspace 2
Standard · VTR-TRACE-20260526Order-Level COA Traceability Standard

The twelve fields every released order should resolve, and the nine links from maker to patient they connect.

You ship to customers and must answer which orders a lot reached.
Aurora Pharma Supply's profile in a sample pharmacy: an API manufacturer in Parsippany, NJ, qualified and signed by Dana Reyes, PharmD on Sep 30, 2026, next review Jan 14, 2027; 2 lots, 2 certificates read, 6 of 11 items on file, 5 owed
Standard · Supplier packetSupplier Packet Diligence Standard

What a reviewed packet contains: six dated elements, up to 20 named checks behind each certificate, and the words a partner may use.

You qualify suppliers, or you are one.
Batches on file, 5, 2 released, each drawn from the day it was made to its use-by date: PY-2026-0922-01 released with 4 Passports, ZN-2026-0929-01 with a recall signal, AS-1180 with no compounding record, CB-2026-1007-01 released and KC-2026-1011-01
Release contract · Methodology v1.0The release gate

What every review must show before anyone relies on it, and the eight reasons the server refuses to let anything leave a lot.

You sign releases, or rely on someone who does.

Start with the question you have to answer.

Four reading paths, each in the order we would hand the documents to you.

Pharmacist in chargeDefend a lot to an inspector.
  1. The release gate
  2. Supplier packet diligence
  3. Methodology
Clinic, med spa or telehealthKnow what you received and where it went.
  1. The sample Passport
  2. Custody, the launch note
  3. Order-level COA traceability
Supplier or API makerAnswer a pharmacy's document request.
  1. Supplier packet diligence
  2. Supplier files in the product
  3. What a report does not do
Counsel or quality consultantCheck what a record proves, and what it does not.
  1. Methodology
  2. For counsel
  3. Why independent

Engine, samples, field notes. Each with who should read it.

The reference pages behind every review, and the records each reader sees. Sample records use the sample workspace; every firm, lot and person in them is fictional.

Methodology

How a document becomes a cited finding. Read if you audit the process, not only the output.

 The evidence engine

Up to 20 named checks, six FDA records and 17 signals. Read if you want to know exactly what is checked.

 What a report does not do

No test of the medicine, no supplier approval. Read if you are about to rely on a record.

 The sample Evidence Passport

The record a patient opens, for order ORD-60412. Read if you dispense to patients, or you are one.

 What a scanned serial resolves to

What a resolving serial does and does not establish. Read if you label medicine or receive it.

 Custody, the launch note

Seven events, three hands, one statement per lot. Read if you release to clinics or receive from pharmacies.

 For counsel

What a record proves, and how to verify it without asking us. Read if you advise a pharmacy or a buyer.

 Why independent

Why the record is kept by a party that sells no badges. Read if you are weighing who should check.

 What a valid certificate carries

23 elements in five groups, each with the source it rests on, and ten questions for one certificate. Read if the law asks you for a valid one.

 Intelligence

17 document-integrity signals, and lots re-matched to FDA enforcement records every hour. Read if one packet review is all you have.

 Trust Center

How a record is received, read, checked, decided and kept, and where the work stops. Read if you have to defend a record later.

 For consultants

Work inside each client's own record, from the grant to one signed PDF. Read if you prepare responses for a facility.

Run one now.

Live today with no account and no card: read your own certificate with the review a workspace runs, check a maker and a substance against the FDA's registries, read FDA's 503A list as printed and checked daily, make a dated receipt for a lot, and verify a Passport or a Seal. The 503B directory and the supplier exposure check return with the registry.

Six tools you can run without an account