Public COA audit
Semaglutide
Audited July 29, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 72
- Confidence
- 85%
- Panels
- 2/7
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- SM202607
- Sample date
- 2026-06-10
- Issue date
- 2026-06-10
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 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
Tested · passed
Bioburden / microbial limits testing.
No Growth (Bacteria), Not Detected (Fungi/Yeast)
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
Tested · passed
Sterility testing where applicable.
Sample Passes Sterility Screen
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.
Limited scope - sterility screening only
This document only provides rapid sterility screening results. No identity confirmation, purity analysis, heavy metals, endotoxin, or residual solvent testing is included. This is a single-panel report, not a comprehensive COA.
Non-regulatory sterility method
Document explicitly states this is a rapid screening method (2 days) and notes that 'for regulatory compliance, full USP <71> sterility testing may be required.' This is a preliminary QC test, not a full sterility validation.
Batch information present
Lot number SM202607 clearly stated with matching dates for receipt and certification (06/10/2026).
Same-day turnaround documented
Sample received and certified on the same date (June 10, 2026), which is plausible for a rapid 2-day screening method that may have been started immediately.
Lab verification not possible
Kovera Labs is identified with professional formatting and an access code/QR code, but no website URL or contact information is provided for independent verification of the lab's credentials or this report.
Professional presentation
Document has clean, professional layout with clear sections, proper branding, and includes a product image. Formatting is consistent with legitimate laboratory reports.
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.