Public COA audit

SLU-PP-332 · GW-501516

Audited July 28, 2026

Evidence suggests fabrication

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

Legitimacy
25
Confidence
88%
Panels
2/7
Purity (printed)
99.24%

Document details

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

Batch / lot
SHREDX-0001
Identity method
LC-MS with UV detection
Sample date
2024-12-27
Issue date
2025-01-04

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

    Tested · passed · core

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

    SLU-PP-332 Conforms

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.24%

  • 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

    Not on this COA · core

    LAL or chromogenic endotoxin assay.

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

  • 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.

  • Identical COA number across multiple compounds

    All three pages share COA #10020 and Security Key BIOLABS2010, but test different compounds (SLU-PP-332, GW-501516, AOD9604) with different batch numbers. Legitimate labs issue unique COA numbers per sample/batch.

  • Inconsistent batch numbering

    Page 1 shows batch SHREDX-0001, pages 2-3 show SHRED-0001. All claim same sample receipt date (12/27/24) and analysis date (1/4/25), suggesting these are from the same submission but with conflicting batch identifiers.

  • Unit inconsistency in quantity measurement

    Page 2 shows specification '5000mcg' but result '4892mg' - mixing micrograms and milligrams in the same field. 4892mg would be 4,892,000mcg, a massive discrepancy. Likely a typographical error but undermines document credibility.

  • Generic lab branding and unverifiable identity

    BioRegen presents as 'Independent Testing, Trusted Results' but provides minimal verifiable information. The verification URL 'bioregen.com/verify' and contact '[email protected]' cannot be independently confirmed as legitimate analytical laboratory infrastructure.

  • Limited testing scope

    Only identity and purity testing performed. No heavy metals, microbial, endotoxin, sterility, or residual solvent testing. While not automatically disqualifying, this is minimal for compounds intended for human research use.

  • Dates within normal range

    Sample received 2024-12-27, analysis conducted 2025-01-04. Both dates are in the past relative to 2026-07-28 and show reasonable 8-day turnaround.

Timing & next steps

Practical follow-ups based on document age and gaps.

  • coa age

    This COA was issued over a year ago (570 days) — consider whether a retest is warranted for this batch.

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.