Public COA audit

Ipamorelin

Audited September 5, 2026

Mostly consistent, with concerns

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

Legitimacy
72
Confidence
88%
Panels
1/7

Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (1/7), 4 soft concerns, and notable note: "Unverifiable lab identity". To improve: include identity, purity, and endotoxin at minimum and prefer labs with a public verification portal.

Document details

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

Batch / lot
IP202606
Sample date
2026-06-10
Issue date
2026-06-10

Original certificate

Embedded copy of the stored COA PDF or image. Download it for your records — PeptIQ’s audit is separate from the lab document itself.

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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 · 1 passed · 0 failed · 0 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 certificate file · core

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

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Purity

    Not on this certificate file · core

    Reported purity percentage for the analyte.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Heavy metals

    Not on this certificate file

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

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Microbial

    Not on this certificate file

    Bioburden / microbial limits testing.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Endotoxin

    Not on this certificate file · core

    LAL or chromogenic endotoxin assay.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Sterility

    Tested · passed

    Sterility testing where applicable.

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

  • Residual solvent / water

    Not on this certificate file

    Residual solvents or water content limits.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

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 on this file

Not on this certificate file. Lowers file thoroughness; a sibling endotoxin/purity report for the same lot may still exist. PeptIQ’s score still factors coverage.

Findings

Evidence-linked observations from this audit.

  • Unverifiable lab identity

    Kovera Labs is not a widely recognized third-party testing laboratory in the peptide industry. No website URL or contact information provided for independent verification.

  • Sterility-only report scope

    This is a single-panel sterility screening report. No identity, purity, endotoxin, heavy metals, or other standard COA panels are included. This may be a supplemental report rather than a comprehensive COA.

  • Rapid screening vs. USP <71>

    Document explicitly states this is a 'rapid screening method' for 'preliminary sterility assessment' and notes that 'full USP <71> sterility testing may be required' for regulatory compliance. This is not a full pharmacopeial sterility test.

  • Same-day turnaround

    Sample received and certified on the same day (06/10/2026). While the 2-day incubation period is stated, same-day certification is unusual for sterility testing which typically requires longer observation periods.

  • Lot number present

    Batch/lot number IP202606 is clearly stated and matches the sample date pattern.

  • Professional presentation

    Report has professional layout with clear sections, QR code for access, and structured data presentation. Includes sample photo.

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.