Public COA audit

GLP-3 (RT) · Retatrutide

Audited July 29, 2026

Consistent with a legitimate COA

Document structure and test panels align with what we expect from authentic lab reports.

Legitimacy
92
Confidence
93%
Panels
5/7
Purity (printed)
99.62%

Document details

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

Batch / lot
RT10-655
Identity method
HPLC-RTM (retention time comparison with reference standard)
Sample date
2026-06-22
Issue date
2026-07-01

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.

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

    Tested · passed · core

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

    Confirmed (Retatrutide)

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.62%

  • Heavy metals

    Tested · passed

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

    As: 0.335 ppm, Cd: 0.1006 ppm, Pb: 0.1005 ppm, Hg: 0.1087 ppm, Cr: 0.1387 ppm

  • Microbial

    Not on this COA

    Bioburden / microbial limits testing.

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

  • Endotoxin

    Tested · passed · core

    LAL or chromogenic endotoxin assay.

    NMT 0.05 EU/mL

  • Sterility

    Tested · passed

    Sterility testing where applicable.

    No Growth

  • 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.

  • High purity with conformity testing

    99.62% purity (batch mean 99.43%, std dev 0.1349%) across 3 conformity samples. HPLC chromatogram shows clean single peak. This is normal for research-grade peptides.

  • Identity confirmed by HPLC-RTM

    Compound confirmed as Retatrutide (GLP-3 RT) by retention time comparison with reference standard.

  • Batch information complete

    Lot RT10-655, COA-2026-R9UV-W, Accession ACC-2026-6114. Net peptide content 10.55 mg (labeled 10 mg).

  • ISO/IEC 17025 accredited lab

    ILS Laboratories, San Diego CA. ISO/IEC 17025 accredited. Verification URL and access code provided. Lab director signature present.

  • Comprehensive testing suite

    Five panels present: purity (HPLC), identity (HPLC-RTM), heavy metals (ICP-MS), sterility (PCR), endotoxin (USP <85>). All tests passed. Microbial culture and residual solvent/water panels not included.

  • Professional presentation

    Two-page format with detailed methodology notes, conformity testing data, QR code for verification, and proper accreditation disclaimers. Formatting is consistent with professional analytical lab standards.

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.