Public methodology

The qualified few worth reviewing—not a list of everyone who can supply.

Provenance starts with a buyer requirement, tests current capabilities against mandatory criteria, labels the evidence and gaps, and controls disclosure before any protected introduction.

For licensed and otherwise authorized commercial operators. Not for patients or consumers. A screen is not product, quality, legal or regulatory approval.

Method: buyer-led, evidence-tagged, controlled disclosure

Last reviewed: 18 October 2026

Five gates

Each gate answers a different failure risk.

01 / Real demand

Is there a decision to serve?

Named buyer, decision-maker, product specification, quantity or credible range, timing, economics and decision process.

02 / Route

Can the responsibilities be mapped?

Destination, importer, manufacturing/processing, testing, permits and any certification or release roles—each tied to a real party and current evidence.

03 / Current evidence

Is this an actual lot or only a capability?

Lot ID, quantity, dates, linked evidence, price basis, validity and decisive unknowns remain distinct from forecasts and catalogues.

04 / Commercial fit

Are the economics comparable?

Same currency, unit, delivery stage and named place; included costs, unknowns, timing, MOQ and terms shown separately.

05 / Protection

Can disclosure proceed safely?

Correct entities, relationship source, fee basis, payer, term, protected parties and permission are recorded before identity or restricted evidence moves.

Boundary / Role

Who performs the regulated work?

Provenance remains a non-custodial commercial originator. Licensed parties import, manufacture, test, certify, release, contract and transact directly.

Illustrative output

A buyer screen built for one decision.

Every fact below is fictional and intentionally non-identifying. The example demonstrates format only.

Synthetic buyer requirement screen

Synthetic example · D0 method view
Destination
Germany
Product
Dried flower; non-irradiated mandatory; total THC target 24–28% on a stated basis
Demand
Illustrative 50 kg monthly recurring requirement; first purchase date to be confirmed
Delivery stage
Buyer needs a documented downstream manufacturing and certification/release path; price comparison must use an equivalent basis
Mandatory evidence
Current lot ID, lot-linked COA, microbiology, GACP basis, allocable kg, quote basis/validity and named route parties
Commercial target
Withheld from the public example; would be recorded with currency, unit, Incoterm and named place
Screen date
18 October 2026 (illustrative only)
Decision rule
Mandatory fail excludes. Unknown requests evidence. No supplier identity is disclosed.
CandidateObserved fitEvidence stateScreen result
SYN-AIllustrative cannabinoid/treatment/quantity fitGACP document reviewed; potency and unallocated kg counterparty-stated; route and comparable delivered cost unknownPossible — evidence needed
SYN-BTreatment conflicts with mandatory non-irradiated requirementIllustrative lot record otherwise completeExclude
SYN-CGeneral capability could fit, but no current lot or linked testingCapability only; availability unknownNot executable

Synthetic example. Not live inventory, a client result or regulatory approval. Codes SYN-A, SYN-B and SYN-C do not correspond to real suppliers. The next decision in this example would be to obtain current lot-linked evidence and a defined downstream cost/route for SYN-A before any identity disclosure.

Evidence-state key

What each label does—and does not—mean.

LabelMeaningLimit
Registry checkedA named public registry record was reviewed on a stated date.Does not prove product fit, capacity, permission outside recorded scope or current transaction acceptance.
Document reviewedA specified document was inspected and its source/date/scope recorded.Does not mean Provenance issued or independently certified it.
Counterparty statedThe attributed party supplied the information.Not converted into independently verified fact.
InferredA working interpretation drawn from available evidence.Never treated as an authority, QP, buyer or supplier decision.
UnknownThe material fact has not been established.Cannot become a pass through expectation or sales language.
Expired / staleThe document, quote or availability is outside its validity or useful freshness.Cannot support a current recommendation until refreshed.

Controlled disclosure

Information moves only as far as the commercial gate allows.

D0 / Internal

Preliminary screen

Internal coded comparison. No external supplier identity, unique facility fact or restricted document.

D1 / Anonymous

Capability summary

Non-identifying, non-unique information for a credible buyer/route, subject to permission.

D2 / Redacted

Controlled evidence

Only after applicable protection, permission and metadata/redaction review. A coded document may still identify a supplier.

D3 / Named

Identity or introduction

Only after the relevant relationship, commercial, route and explicit release gates are satisfied.

Confidentiality is not fee protection. An NDA may govern confidentiality, but the commercial relationship, payer, fee base, trigger, term, protected parties and exceptions must be addressed separately before an introduction.

Buyer output

Short, dated and decision-ready.

Requirement version

The source-backed requirement, mandatory criteria, allowed flexibility and date.

Up to three candidates

Why each passes, fails or remains unknown, with source and availability dates.

Comparable economics

Equivalent delivery stage, inclusions, unpriced items and exchange-rate source/date where used.

Evidence gaps

The smallest set of facts needed to decide whether further diligence is justified.

Disclosure state

What can be shared, what remains controlled and which protection or permission is missing.

One next decision

The buyer, supplier or Provenance owner and the next update date—rather than a vague follow-up.

Method sources

Technical evidence is checked against primary records.

Method limit: the screen organizes commercial and evidence questions. It does not replace the buyer's, supplier's, importer's, manufacturer's, laboratory's, QP's, legal counsel's or authority's decision.

Use the method

Bring one real buying requirement.

The free first screen returns a credible fit worth diligence, the missing information needed to decide, or a no-fit answer.

Submit the requirement →