Noverix Verify
We don’t sell peptides for human use. We help researchers and organizations evaluate analytical documentation, coordinate third-party testing, and verify lot-level quality records for research-use-only materials.
Request a Verification See a sample reportNoverix Verify is led by an analyst with hands-on training across analytical, microbiology, and R&D laboratories at AbbVie, Bristol Myers Squibb, and Thermo Fisher Scientific — trained on HPLC, LC-MS, and analytical-data review.
View LinkedIn profile →The peptide boom has a trust problem
Demand is exploding — and so is questionable product. Buyers and labs increasingly can’t tell what’s real.
Certificates with no identifiable lab, no method listed, or recycled lot numbers.
Purity does not prove identity — a “99% pure” sample can still be the wrong molecule.
Net content and concentration that don’t match what the label claims.
No way to tie a vial back to a real, dated, third-party test result.
Services
Start with a document review, or have us coordinate full third-party testing. Pricing is per item; testing is quoted to the lab scope.
COA Review
- Is the COA structurally legitimate?
- HPLC / LC-MS methods present & appropriate
- Lot number, date & lab-identity check
- Molecular-weight & purity sanity check
- Red-flag summary
Full Lot Verification Report
- Everything in COA Review, plus:
- Supplier & document cross-check
- Third-party testing recommendation
- Risk score
- Premium branded PDF report
Third-Party Testing Coordination
- We coordinate accredited external labs
- HPLC purity · LC-MS identity · net content
- Heavy metals / endotoxin / sterility as applicable
- You ship the sample — we manage the rest
- Clean report + optional QR lot page
What a Noverix COA review checks
How it works
Send your COA, supplier info, or sample details.
We assess it against HPLC / LC-MS analytical-quality criteria.
A clean PDF report — with an optional QR lot-verification page.
Frequently asked questions
What does Noverix Verify actually do?
We provide independent review of analytical documentation, coordinate third-party testing, and verify lot-level quality records for research-use-only materials. We do not sell peptides for human use.
Who reviews my documentation?
Your documentation is reviewed by a Noverix analyst with hands-on training across analytical, microbiology, and R&D laboratories at AbbVie, Bristol Myers Squibb, and Thermo Fisher Scientific, including HPLC, LC-MS, and analytical-data review.
What is the difference between a COA Review and a Full Lot Verification Report?
A COA Review ($20) is a focused assessment of a single certificate of analysis. A Full Lot Verification Report ($249) adds a supplier and document cross-check, a third-party testing recommendation, a risk score, and a premium PDF report.
Do you test the product itself, or only the paperwork?
A document review evaluates the COA and supporting paperwork. To confirm what is physically in a vial, we coordinate independent third-party laboratory testing, such as HPLC purity and LC-MS identity, and present the results in a clean report.
How long does a review take?
COA reviews are typically returned within one to two business days. Third-party testing timelines depend on the laboratory and the scope of testing requested.
Can you guarantee that a peptide is real or safe?
No. Our reports reflect a professional review against analytical-quality criteria and are not a guarantee of identity, purity, safety, or fitness for any purpose. All materials are research-use-only, and we do not provide medical, dosing, or clinical guidance.
Are your reviews independent, and is my information kept confidential?
Yes. Reviews are independent of the suppliers being evaluated, and the documents and details you share are kept confidential.
Request a Verification
Tell us what you need reviewed. We typically reply within one business day with next steps and a quote.