Public COA audit
Humanin
Audited July 28, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 72
- Confidence
- 83%
- Panels
- 1/7
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- HP20250805
- Issue date
- 2025-09-19
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.
Endotoxin testing present
Document is a specialized endotoxin testing report using Pierce Chromogenic LAL assay. Result < 0.20 EU/mL passes stated threshold.
Single-panel report
This is an endotoxin-only report, not a comprehensive COA. Identity, purity, heavy metals, microbial, sterility, and residual solvent panels are absent. This is typical for supplemental testing but incomplete as a standalone COA.
Batch/LOT number present
LOT #: HP20250805 clearly stated for Humanin product.
Lab verification unclear
BioRegen lab name, contact email, and website are provided with validation key PEPPART901, but independent verification of this lab's accreditation or existence was not performed. QR code and validation key suggest verification mechanism exists.
Interpretation inconsistency
Interpretation states result '< 0.20 EU/mL indicates endotoxin content is below the acceptable threshold of 0.1 EU/mL' — but 0.20 is above 0.1. This appears to be a typo (likely meant '< 0.02' or threshold is 0.2). The conclusion 'Passes' is stated but the logic is contradictory.
Professional presentation
Document has professional layout with clear tables, reagent traceability (Thermo Fisher kit A39553), controls documented, and analyst signature line.
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.