Public COA audit

CJC-1295 · Ipamorelin

Audited July 28, 2026

Evidence suggests fabrication

Multiple signals on this document conflict with known lab formats or verification patterns.

Legitimacy
15
Confidence
92%
Panels
1/7

Scored poorly because audit signals point to fabrication or reused paperwork, limited panel coverage (1/7), 4 critical findings, and notable note: "Future Date". To improve: replace this file with an original lab certificate that verifies on the lab portal and include identity, purity, and endotoxin at minimum.

Document details

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

Batch / lot
N260710-001
Identity method
HPLC
Issue date
2026-07-17

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

    Tested · passed · core

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

    CJC-1295: 9.1 mg, Ipamorelin: 8.8 mg

  • 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

    Not on this certificate file

    Sterility testing where applicable.

    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.”

  • 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.

  • Future Date

    Issue date is 2026-07-17, which is in the future. This is a major red flag indicating the document is fabricated or the date has been altered.

  • Unverifiable Laboratory

    Qalitex Inc. with accreditation AGS-US050824-1 cannot be independently verified. No verification URL or QR code destination provided. The accreditation number format is non-standard.

  • Minimal Testing

    Only HPLC assay testing performed. No purity percentage, identity confirmation beyond mass, heavy metals, microbial, endotoxin, sterility, or residual solvent testing. This is extremely limited for a peptide COA.

  • No Purity Data

    Document reports mass quantities (8.8 mg, 9.1 mg) but provides no purity percentage, which is essential for peptide quality assessment.

  • Mass-Only Verification

    Identity verification appears to be mass-based only via HPLC. No retention time, molecular weight confirmation, or other identity markers provided.

  • Generic Template

    Document uses a generic template design with minimal specific technical detail. Client address fields are blank or contain only commas.

  • Batch Information Present

    Batch number N260710-001 and lot number SP26-CIV16 are clearly stated.

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.