Public COA audit

Retatrutide

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
RT202607
Sample date
2026-06-09
Issue date
2026-06-09

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.

    Bacteria: No Growth; Fungi/Yeast: Not Detected

  • 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.

  • Limited scope - sterility only

    This is a single-panel sterility screening report, not a comprehensive COA. Missing identity, purity, heavy metals, endotoxin, and residual solvent testing. This is legitimate for sterility verification but incomplete for full peptide characterization.

  • Rapid screening method

    Document explicitly states this is a 2-day rapid screening method, not full USP <71> sterility testing. Suitable for QC but may not meet regulatory compliance requirements.

  • Batch number present

    Lot number RT202607 clearly documented

  • Same-day turnaround

    Sample received and certified on same day (06/09/2026), which is plausible for rapid screening methods

  • Lab verification not possible

    Kovera Labs name is present but no website URL or contact information provided for independent verification. QR code present but cannot be scanned from static image.

  • Professional presentation

    Clean, professional layout with clear branding, structured data presentation, and appropriate technical detail for the test type

  • Sterility results clear

    Both bacterial (aerobic/anaerobic) and fungal/yeast testing show negative results with clear pass status

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.