Public COA audit

BPC-157/TB-500

Audited July 29, 2026

Mostly consistent, with concerns

Several fields check out, but we found issues worth reviewing before you rely on this document.

Legitimacy
72
Confidence
85%
Panels
2/7

Document details

Fields extracted from the certificate — not order or payment data.

Batch / lot
BB202605
Sample date
2026-04-21
Issue date
2026-04-21

7-panel checklist

Had data + good, had data + bad, reported without pass/fail, or missing. Missing lowers thoroughness — you decide whether that panel matters; PeptIQ’s score still factors coverage.

2 of 7 present · 2 passed · 0 failed · 0 reported · 5 missing

Missing is a thoroughness gap — not automatically bad. PeptIQ’s legitimacy score still weighs panel coverage; you can down-weight panels that don’t matter for your use case.

  • Identity

    Not on this COA · core

    Compound identity confirmed (e.g. HPLC, mass spec).

    No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.

  • Purity

    Not on this COA · core

    Reported purity percentage for the analyte.

    No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.

  • Heavy metals

    Not on this COA

    Lead, arsenic, cadmium, mercury, or similar limits.

    No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.

  • Microbial

    Tested · passed

    Bioburden / microbial limits testing.

    No Growth (Bacteria), Not Detected (Fungi/Yeast)

  • Endotoxin

    Not on this COA · core

    LAL or chromogenic endotoxin assay.

    No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.

  • Sterility

    Tested · passed

    Sterility testing where applicable.

    No microbial growth detected

  • Residual solvent / water

    Not on this COA

    Residual solvents or water content limits.

    No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.

How to read this

Had data · good

Panel present with a pass (or clear acceptance).

Had data · bad

Panel present with a fail — a concrete quality signal.

Had data · unclear

Value reported without an explicit pass/fail mark.

Missing

Not on this certificate. Lowers thoroughness; you decide if that panel matters for your use case. PeptIQ’s score still factors coverage.

Findings

Evidence-linked observations from this audit.

  • Sterility-only report

    This is a specialized sterility screening report only. No identity confirmation (HPLC/MS), purity analysis, heavy metals, endotoxin, or residual solvent testing is included. This is a supplemental test, not a comprehensive COA.

  • Lab verification needed

    Kovera Labs is not a widely recognized third-party peptide testing laboratory. No verification URL or independent contact information provided. QR code present but destination unknown.

  • Same-day turnaround

    Sample received and certified on the same day (04/21/2026) despite methodology stating 14-day incubation period. This timeline inconsistency raises questions about test completion.

  • Professional presentation

    Document has clean formatting, proper headers, methodology description, and includes sample photo with matching batch number visible on vial.

  • Batch number present

    Lot number BB202605 clearly stated and visible on product vial in photograph.

  • Rapid screening caveat

    Document explicitly states this is a 'preliminary sterility assessment' and notes 'For regulatory compliance, full USP <71> sterility testing may be required.' This is a screening test, not definitive sterility certification.

PeptIQ COA reports analyze document content and publicly verifiable lab signals. They are educational and not a guarantee of product quality, legality, or safety. Always consult a qualified professional before making health decisions. We never publish purchase prices, shipping details, or uploader identity.