Public COA audit

Retatrutide

Audited July 28, 2026

Incomplete documentation

Missing panels or key metadata — not enough evidence to treat this as a full certificate.

Legitimacy
45
Confidence
82%
Panels
1/7

Document details

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

Batch / lot
RP20250929
Issue date
2025-10-03

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.

1 of 7 present · 0 passed · 0 failed · 1 reported · 6 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

    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 · result on file · core

    LAL or chromogenic endotoxin assay.

    35.8 EU/mL

  • Sterility

    Not on this COA

    Sterility testing where applicable.

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

  • 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.

  • No purity testing

    This COA contains only endotoxin testing. No HPLC, MS, or other purity/identity analysis is present, which is essential for peptide quality verification.

  • No identity confirmation

    No mass spectrometry, NMR, or other identity verification method is documented. Cannot confirm the compound is actually Retatrutide.

  • Single-panel COA

    Only endotoxin testing (USP <85>) is performed. A comprehensive COA for research peptides typically includes identity, purity, and multiple safety panels.

  • Endotoxin result interpretation unclear

    Result shows 35.8 EU/mL with no explicit pass/fail statement. Comment references 'USP limit 5 EU/kg/hr' but does not state whether this sample meets requirements for its intended use.

  • No sample collection date

    Only publication date (2025-10-03) is provided. Sample receipt or collection date is not documented.

  • Lab information present

    TrustPointe Analytics LLC with full contact details, verification URL (TrustPointeLIMS.com), and verification key (F1OX9VJR4D59) provided.

  • Professional presentation

    Document has professional formatting with QR code, signatures from President and Managing Director, and clear layout.

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.