Resources
Read how the check works before you rely on it.
The standards, the SOPs, the worked examples, the sample records, and the free tools, all published and all dated.
Standards
The documents that define the work.
Published, versioned, and dated. Read them before you rely on an output.
Standard
VTR-TRACE-20260526
Order-Level COA Traceability Standard
The twelve-field minimum operating record, the five-step flow from supplier packet to customer proof, and the line between what an operator sees and what a customer is shown.
Standard
Supplier Packet Diligence Standard
Where the document review sits relative to a QMS or an ERP, what the memo contains, how the evidence index grows, and the exact language a partner may use about a reviewed packet.
Methodology
v1.0 . April 30, 2026
Methodology v1.0
What is checked, the public sources it is checked against, and how the work is governed.
Limitations
What a report does not do
Not a safety assessment, not product testing, not a provenance proof, not a purchase recommendation.
Release gate
Each Veritura deliverable must be understandable in under sixty seconds.
A buyer should not need to decode a dashboard or read a wall of text. Six gates are required. If any gate is missing, the output stays in review instead of pretending to be enterprise-ready.
Gate 01
Executive verdict
The operator can state the record posture without caveat hunting.
Gate 02
Evidence map
Every material claim points to a source file, row, field, or explicit limitation.
Gate 03
Evidence replay
The artifact shows how intake, extraction, reconciliation, QA, release, and archive state produced the decision.
Gate 04
Risk boundary
The artifact excludes product approval, safety, legal, medical, and purchase language.
Gate 05
Next action
The client knows exactly what to ask, hold, route, review, or release next.
Gate 06
Export package
The record can be forwarded, archived, audited, or attached to a workspace.
No Veritura output ships as customer-safe until the verdict, evidence map, replay path, boundary language, next action, and export package are present and consistent with the source record.
Sample output
What a buyer sees before they buy.
The full output contract, on real documents, with the evidence trail attached.
Customer record
The passport a patient opens
The customer-safe record from a seal scan: the completeness band in plain words, the origin of the certificate line, and what it explicitly does not establish. No posture word and no score.
Operator record
The full Evidence Passport
The same lot as the workspace sees it: posture and origin on separate axes, every document with its own origin, the release gates, and the boundary block.
Seal check
What a scanned serial resolves to
The verification panel a person meets after scanning the QR on a vial, and the list of what a resolving serial does and does not establish.
Check catalog
Every signal the engine records
The published check catalog with each signal, what it detects, and the lane it belongs to, plus the four evidence lanes and the three states each can end in.
The record
An Evidence Passport, end to end.
Rendered here from local sample data so you can read the whole record without an account.
Evidence Passport
Semaglutide (base) API
Evidence posture
Evidence posture: ClearThe document set met the configured policy. It describes the paperwork, not the medicine.
Certificate of analysis
Source-confirmedThe issuing laboratory confirmed issuance through the recorded verification route.
- Order
- PO-DEMO-0413
- Lot
- LOT-7741-A
- Supplier
- Aurora Pharma Supply
- Quantity
- 250 g
- Received
- July 22, 2026
- Released
- July 23, 2026
- Passport issued
- July 23, 2026
- Methodology
- v1.0 · April 30, 2026
Documents on file
6
- Source-confirmed
Certificate of analysis
COA-7741-A.pdf · Issuing laboratory confirmed issuance through the recorded route
- Veritura evaluated
Certificate of conformance
CoC-7741.pdf · Required identity, lot, and date fields present
- Veritura evaluated
Safety data sheet
SDS-SEMA-04.pdf · Current revision on file
- Operator attested
GMP certificate
GMP-AUR-2026.pdf · Supplied by the operator
- Operator attested
Receiving inspection
Recorded in workspace · Container and label checked at receipt
- Veritura evaluated
Shipment label
LBL-7741-A.jpg · Lot identifier matches the certificate of analysis
What this record does not establish
- Documentation diligence only. No product was tested and no supplier was approved.
- Absence of a public-source match is not proof of absence.
- Produced under methodology v1.0, April 30, 2026.
Guides
Practitioner reading.
Written for the person who has to defend the decision.
Position
Why independent
Transparency shows a document. An independent check tests it. A player cannot be the referee.
Free tools
Run one now.
Each one is live on veritura.co. No account, no card.
Public tools
Five checks you can run without an account
FDA source check, the 503B directory, the supplier exposure self-check, the claim checker, and seal verification. Each one states what it takes, what it returns, and what its answer does not mean.
Not found in the snapshot never means not registered. It means the name did not match the captured list.
What is not on this page.
There are no case studies or customer stories here. No customer has given written permission to be named, and an anonymised success story is not evidence of anything. What is published is the methodology, the standards, the sample output, and the tools above.
Start on your own documents.
Every standard, SOP and sample above is published. The workspace is where they get applied to a packet you actually have to decide on.
Redact patient information and nonessential commercial terms before sending materials.