Public COA audit

Semaglutide

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
1/7

Document details

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

Batch / lot
SM202607
Issue date
2026-06-10

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 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

    Not on this COA

    Bioburden / microbial limits testing.

    No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.

  • Endotoxin

    Tested · passed · core

    LAL or chromogenic endotoxin assay.

    < 0.20 EU/mL

  • Sterility

    Not on this COA

    Sterility testing where applicable.

    No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.

  • 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.

  • Single Panel Only

    This COA contains only bacterial endotoxin testing. No identity confirmation (HPLC/MS), purity analysis, heavy metals, microbial, sterility, or residual solvent testing is included. This is a partial analysis report, not a comprehensive COA.

  • No Purity Data

    No HPLC or other purity measurement is provided. Cannot verify compound purity or identity from this document alone.

  • No Identity Confirmation

    No mass spectrometry, HPLC retention time, or other identity verification method is documented. The compound name is stated but not analytically confirmed.

  • Analysis Date Valid

    Analysis date of 2026-06-10 is within acceptable range (before current date of 2026-07-29).

  • Lab Information Present

    Testing lab identified as Kovera Labs with verification URL (koveralabs.com/verify), sample ID KVR-2026-D8F3B3, and access code 52570D provided.

  • Batch Number Present

    Lot/Batch number SM202607 clearly documented.

  • Professional Presentation

    Document follows standard analytical testing report format with clear sections, methodology, results, controls, and authorization signature from Lab Director Lemar Arghandiwal.

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.