Public COA audit

Tirzepatide · GLP TZ

Audited September 5, 2026

Evidence suggests fabrication

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

Legitimacy
15
Confidence
92%
Panels
3/7
Purity (printed)
99.784%

Scored poorly because audit signals point to fabrication or reused paperwork, limited panel coverage (3/7), 4 critical findings, and notable note: "Non-existent testing laboratory". 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
GT10-032026-1
Identity method
HPLC with UV Detection Coupled with Mass Spectrometry
Sample date
2026-03-10
Issue date
2026-03-11

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.

3 of 7 present · 3 passed · 0 failed · 0 reported · 4 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).

    GLP TZ confirmed

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.784%

  • 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

    Tested · passed · core

    LAL or chromogenic endotoxin assay.

    Pass (Replicate 1 and 2)

  • 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.

  • Non-existent testing laboratory

    Freedom Diagnostics does not appear to be a legitimate analytical testing laboratory. The website FreedomDiagnosticsTesting.com does not resolve to a known analytical chemistry lab. No accreditation information (ISO 17025, GMP, etc.) is provided.

  • Unprofessional document design

    The COA uses consumer-grade design elements including a stock photo of a vial with printed label, inconsistent formatting, and lacks professional laboratory report structure. Legitimate analytical labs use standardized, professional templates.

  • Abbreviated compound naming

    The compound is listed as 'GLP TZ' rather than the full chemical name 'Tirzepatide' or proper IUPAC nomenclature. Professional COAs typically use complete chemical identifiers.

  • Missing critical safety panels

    No heavy metals, microbial contamination, sterility, or residual solvent/water content testing is documented. Comprehensive peptide analysis typically includes these panels.

  • Missing accreditation and quality statements

    No ISO 17025 accreditation, laboratory certifications, or quality assurance statements are present. The disclaimer focuses on limiting liability rather than affirming analytical standards.

  • Product photo inclusion

    The inclusion of a product vial photograph is highly unusual for analytical COAs, which typically only show analytical data and chromatograms. This suggests a marketing document rather than a laboratory report.

  • Very rapid turnaround

    Sample received 03/10/2026 and reported 03/11/2026 represents a 1-day turnaround for HPLC-MS and endotoxin testing, which is unusually fast for comprehensive analysis.

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.