Public COA audit
Retatrutide
Audited September 5, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 92
- Confidence
- 95%
- Panels
- 1/7
Scored high because the document is mostly consistent but carries soft concerns, limited panel coverage (1/7), and 1 soft concern. To improve: include identity, purity, and endotoxin at minimum.
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- RT202607
- Issue date
- 2026-06-09
Original certificate
Embedded copy of the stored COA PDF or image. Download it for your records — PeptIQ’s audit is separate from the lab document itself.
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 certificate file · core
Compound identity confirmed (e.g. HPLC, mass spec).
No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”
Purity
Not on this certificate file · core
Reported purity percentage for the analyte.
No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”
Heavy metals
Not on this certificate file
Lead, arsenic, cadmium, mercury, or similar limits.
No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”
Microbial
Not on this certificate file
Bioburden / microbial limits testing.
No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”
Endotoxin
Tested · passed · core
LAL or chromogenic endotoxin assay.
< 0.20 EU/mL
Sterility
Not on this certificate file
Sterility testing where applicable.
No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”
Residual solvent / water
Not on this certificate file
Residual solvents or water content limits.
No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”
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 on this file
Not on this certificate file. Lowers file thoroughness; a sibling endotoxin/purity report for the same lot may still exist. PeptIQ’s score still factors coverage.
Findings
Evidence-linked observations from this audit.
Endotoxin testing present
Document shows comprehensive bacterial endotoxin testing using kinetic chromogenic LAL assay per USP <85>. Result < 0.20 EU/mL meets acceptance limit ≤ 0.5 EU/mL. Positive and negative controls passed.
Limited scope report
This is an endotoxin-only testing report. No purity, identity, heavy metals, microbial, sterility, or residual solvent panels are present in this document. This may be part of a split testing approach where other panels are reported separately.
Lab identification clear
Kovera Labs clearly identified with lab director signature (Lemar Arghandiwal), sample ID KVR-2026-CD3187, access code E59D8D, and verification URL koveralabs.com/verify provided.
Analysis date documented
Analysis date 06/09/2026 is clearly stated and is on or before the current date (2026-09-05).
Batch information complete
Lot/Batch RT202607 clearly documented with product name Retatrutide, strength 24 mg, condition lyophilized.
Professional presentation
Document follows standard analytical testing report format with clear sections for methodology, results, controls, interpretation, and authorization. QR code and verification URL included for authenticity checking.
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.