AI Provider Trust Registry evidence verified as of 2026-08-19

Methodology

This registry is an evidence index, not a legal determination. It records what public documents say and don’t say about each offering, with a primary-source link, a verbatim quote, and the date the value was last confirmed on every cell. It never answers “can I use this legally”, that is a question for your counsel, informed by evidence like this.

How cells are researched and graded

Cells are researched and graded by autonomous LLM agents working against a published rubric, not filled in by hand. A daily process rolls through the registry, oldest cells first. For each cell, a verifier agent searches for the provider’s own authoritative page, fetches it (rendering JavaScript trust portals and reading PDFs), and grades the cell against the rubric, which fixes the meaning of every value, the rules for which sources count as authoritative, and the per-dimension precedents. It records a value only on evidence it actually fetched: a primary-source link, a verbatim quote from that page, a confidence, and the date. It is instructed never to assert a fact from memory.

Every grade is then audited by a second, independent agent (a different model) that re-reads the cited page and checks three things, that the source is the provider’s own authoritative domain, that the quote is really on it, and that the value fits the evidence, and corrects clear mistakes. Anything the agents genuinely cannot verify, because no authoritative page exists or the page will not load, is flagged for human review rather than guessed. Corrections sent in by the public are applied by a human on top of this.

What a cell means

Every cell grades the public evidence for the compliance-favorable answer to a fixed question, for example, “will they sign a HIPAA BAA covering this offering?” The value is a coarse index for scanning; the note and source on each cell are the actual evidence, read them. The grades:

StatusMeaning
yes_publicPublicly verifiable from the provider’s own documents.
yes_sales_gatedThe provider states it exists, but the artifact (report, agreement, feature) requires a sales conversation, NDA, or enterprise tier.
yes_platform_onlyAvailable, but only through a particular deployment or platform path.
partialSome of the question is publicly satisfied; a material part is not.
no_public_evidenceWe could not verify the favorable answer from public sources. This is not the same as “no”: the artifact may exist behind an NDA or an enterprise agreement. The note says what we checked.
no_verifiedWe checked an authoritative, complete source and the answer is a confirmed no, not merely unverified. Used where such a source exists, for example the European Commission’s own GPAI Code of Practice signatory list: a developer absent from it has not signed, which is a stronger and more useful statement than “no public evidence.”
not_applicableThe question doesn’t apply to this row (for example, GPAI Code status for a serving platform that is not the model’s provider).
unclearSources exist but don’t settle the question.
conflicting_sourcesPublic sources disagree. The cell’s notes say how.

Verification discipline

On audit reports (SOC 2, ISO)

Essentially every SOC 2 Type II report is confidential and released under NDA, so “can you download the report” is true of almost nobody and tells you nothing. What actually differs between providers is whether the provider publicly documents that this specific offering is inside the audit scope, and that is what these cells record.

So an offering being sales-gated here is not a criticism of the provider’s security. It means you cannot confirm the coverage of the exact thing you are buying without asking them for it.

On the EU AI Act columns

The GPAI Code of Practice is voluntary. A provider absent from the signatory list may demonstrate compliance by alternative means. The registry records signatory status (full, partial by chapter, or absent from the list) and whether an Article 53 training-data summary is published, it never claims a provider “has no EU compliance path” or is “non-compliant.”

Corrections policy

If you work for a provider listed here and a cell is wrong or stale: send the primary source that corrects it. Corrections with evidence are folded in within days, credited in the changelog, and the cell’s verification date is refreshed. Email [email protected] with the source linked. Disputes about grading (rather than facts) get a note in the cell rather than a silent change.

Use the data

data.json is the whole registry, free, machine-readable. Attribution with a link is required. If you need dated, procurement-attachable evidence snapshots or a licensed feed, subscribe in the footer and say so - that demand signal is what decides whether those get built.