Public COA audit

Retatrutide

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), 2 soft concerns, and notable note: "Endotoxin testing present". To improve: include identity, purity, and endotoxin at minimum.

Document details

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

Batch / lot
RP20250929
Issue date
2025-10-03

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 · 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 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

    Tested · result on file · core

    LAL or chromogenic endotoxin assay.

    35.8 EU/mL

  • 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.

  • Endotoxin testing present

    USP <85> bacterial endotoxin test performed with result 35.8 EU/mL, including spike recovery (76%) and CV data. This is an endotoxin-scoped report only.

  • Limited scope - endotoxin only

    This COA contains only endotoxin testing. No purity, identity, heavy metals, microbial, sterility, or residual solvent panels are present. The sample name includes 'ENDO' suffix suggesting this is a split report focused on endotoxin testing only.

  • No explicit pass/fail stated

    Endotoxin result of 35.8 EU/mL is reported with USP limit reference of 5 EU/kg/hr, but no clear pass/fail determination is stated on the document.

  • Issue date valid

    Published date 2025-10-03 is within acceptable range (before 2026-09-05).

  • Batch/lot number present

    Client SID RP20250929 clearly identified.

  • Lab identification complete

    TrustPointe Analytics LLC with full address, contact information, and verification URL provided.

  • Professional presentation

    Document includes QR code for verification, signatures from President and Managing Director, and structured data presentation.

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.