Public COA audit

DSIP

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
85%
Panels
2/7

Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (2/7), 2 soft concerns, and notable note: "Sterility-only report". 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
DS202605
Issue date
2026-05-07

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.

2 of 7 present · 2 passed · 0 failed · 0 reported · 5 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

    Tested · passed

    Bioburden / microbial limits testing.

    No microbial growth detected during the 14 day incubation period

  • 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 detected (aerobic and anaerobic)

  • 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.

  • Sterility-only report

    This is a specialized sterility/microbial screening report only. It does not include identity, purity, endotoxin, heavy metals, or residual solvent testing. This may be one component of a multi-part COA suite for lot DS202605.

  • Lab verification not possible

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

  • Batch number present

    Lot/Batch DS202605 clearly stated

  • Sterility testing methodology detailed

    BacT ALERT automated system with 14-day aerobic/anaerobic incubation and colorimetric CO2 detection is a legitimate and recognized sterility testing method. Results show no microbial growth.

  • Professional presentation

    Document has professional layout, clear methodology description, appropriate disclaimers about batch-level sterility, and 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.