Trust center
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. Here's exactly how the work is governed.
Every report stamps the methodology version (v1.0 · 2026-04-30). Material changes require a new version and a public changelog entry.
Every reviewed document is hashed and assigned an evidence ID, preserved in the report so the file can be reconstructed at inspection time.
AI assists with first-pass extraction and drafting; a human reviews the final language before anything is delivered or relied upon.
Professional liability / errors-and-omissions coverage supports the documentation-diligence work. It does not convert any report into approval, safety coverage, legal advice, or regulatory sign-off.
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.
If evidence changes, the record is corrected, transparently, with the basis for the change preserved. Findings are tied to evidence, not opinion.
Methodology
A mechanical, repeatable process, so two reviewers reach the same record, and an inspector can follow it.
Operating boundary
Rank vendors · recommend purchases · test physical material · certify products · provide medical, legal, or regulatory advice · determine legality · confirm FDA approval, clearance, or registration.
Document what is present, conflicting, missing, changed, or not verified in reviewed materials, with cited evidence, hashes, limits, and the next supplier question, for a human to decide.
Run a check, or talk to us about covering your supplier base.