Public COA audit
CJC-1295 no DAC/Ipamorelin Blend
Audited July 29, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 92
- Confidence
- 93%
- Panels
- 1/7
Document details
Fields extracted from the certificate — not order or payment data.
- Sample date
- 2025-04-09
- Issue date
- 2025-04-09
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.
< 0.01 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 performed
Chromogenic LAL assay performed with proper controls, result < 0.01 EU/mL passes acceptable threshold of 0.1 EU/mL
Limited testing scope
This is a single-panel endotoxin report only. No identity, purity, heavy metals, microbial, sterility, or residual solvent testing is included on this document
No batch/lot number provided
Document does not specify a batch or lot number for traceability
Professional presentation
BioRegen branding, validation key (BIOLABS2010), report ID (BL-ENDO-250409-001), QR code for verification, and analyst signature present
Test date documented
Test performed and report dated 04/09/2025, which is within normal timeframe
Proper methodology documentation
Kit product number (A39553 Thermo Fisher), endotoxin standard (E.coli O111:B4), detection range (0.01-1.0 EU/mL), and plate reader specifications included
Timing & next steps
Practical follow-ups based on document age and gaps.
coa age
This COA was issued over a year ago (476 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.