Public COA audit
Pinealon
Audited July 29, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 92
- Confidence
- 88%
- Panels
- 1/7
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- PN202603
- Issue date
- 2026-04-01
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.
< 0.03 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
Comprehensive bacterial endotoxin analysis using USP <85> kinetic chromogenic LAL assay with proper controls and spike recovery validation (98%). Result < 0.03 EU/mL passes acceptance limit of ≤ 0.5 EU/mL.
Limited scope COA
This is a single-panel endotoxin-only report. No identity, purity, heavy metals, microbial, sterility, or residual solvent testing is included. This is common for specialized endotoxin testing but means this COA alone does not establish compound identity or purity.
Professional lab presentation
Kovera Labs report shows professional formatting with detailed methodology, controls, QC metrics (CV%, spike recovery), and dual authorization by QC Analyst and Quality Director.
Batch information present
Lot/Batch PN202603 clearly identified with product name (Pinealon), strength (20 mg), and condition (Lyophilized).
Verification system provided
Document includes verification URL (koveralabs.com/verify), sample ID (KVR-2026-E72260), and access code (97E7D4) for independent verification.
Cannot independently verify lab
While the document appears professionally formatted, independent verification of Kovera Labs' existence and the validity of the verification URL/access code cannot be confirmed from the document alone.
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.