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COA Testing

One-time 7 Panel testing for a single sample submission.

$ 249 / Test

What's included

  • Identity Verification
  • Purity Analysis
  • Quantity Verification
  • 7 Panel COA Report
Lab Testing Resource Guide

Your complete guide to PeptideValidation.com lab testing

Explore the core analytical methods used to evaluate peptide purity, identity, sterility, and bacterial endotoxins, together with our testing standards, certification framework, and applied testing resources.

4 Core Testing Guides Independent Laboratory Partners Batch-Specific COAs Independent, Third-Party Testing

Four core methods used in peptide quality evaluation

Purity, identity, sterility, and endotoxin testing answer different quality questions. Each guide explains the method, the information a laboratory report should contain, and the limits of the conclusions that can be drawn.

Purity Analysis

HPLC Peptide Testing

214nm UVC18 columnPurity profiling

Reverse-phase HPLC separates a peptide from synthesis impurities and quantifies purity as a percentage of total peak area. It is a primary method for purity profiling, but it does not confirm molecular identity on its own.

  • Measures purity via C18 hydrophobicity separation
  • Detects deletion peptides & oxidized residues
  • Must be paired with LC-MS for identity
Read the full HPLC guide
Identity Verification

LC-MS Peptide Testing

Mass analysisESI ionizationMS/MS available

Mass spectrometry measures the exact molecular mass of a peptide and compares it to the theoretical weight of the intended sequence and helps determine whether the detected compound is analytically consistent with the intended peptide.

  • Confirms mass via multiply-charged ion deconvolution
  • Detects wrong sequences, oxidation, deamidation
  • Required alongside HPLC — never a substitute
Read the full LC-MS guide
Microbial Safety

Sterility Testing

USP <71>14-day cultureFTM + SCDM

Confirms a batch is free of viable bacteria, fungi, and yeast via 14-day culture in two growth media. This method evaluates viable microbial contamination in the tested sample.

  • FTM targets anaerobic/aerobic bacteria
  • SCDM targets fungi, yeast & aerobes
  • Results are interpreted against the laboratory protocol
Read the full sterility guide
Pyrogen Safety

Endotoxin Testing (LAL)

USP <85>USP <85> framework3 LAL methods

The LAL assay detects bacterial lipopolysaccharides that may remain even when viable organisms are not detected. This is a separate quality question from purity, identity, and sterility.

  • Gel-Clot, Turbidimetric & Chromogenic methods
  • Acceptance criteria depend on the application
  • A sterile batch can still fail endotoxin
Read the full endotoxin guide

Method comparison, at a glance

No single method answers every quality question. This table shows the primary purpose of each test and the areas it does not independently evaluate.

Method Confirms Purity Confirms Identity Detects Microbes Detects Endotoxins Full Guide
RP-HPLC ✔ Primary ✘ No ✘ No ✘ No HPLC Guide →
LC-MS (ESI) ◑ Partial ✔ Primary ✘ No ✘ No LC-MS Guide →
Sterility (USP <71>) ✘ No ✘ No ✔ Primary ✘ No Sterility Guide →
Endotoxin / LAL (USP <85>) ✘ No ✘ No ✘ No ✔ Primary Endotoxin Guide →

Standards, certification & applied testing

Beyond the four methodology guides, these two resources cover who we are and how the science applies to a real, in-market peptide.

Company · Standards

About PeptideValidation.com

Peptide validation means checking the claim, not repeating it. Learn how our independent testing, COA verification, and vendor certification framework works — and why a logo and a PDF aren't validation.

About & Certification Standards
Case Study · Blog

Retatrutide Purity Testing

A polished COA doesn't prove a retatrutide sample contains what its label claims. See how HPLC and LC-MS are applied together to separate purity, identity, and content claims for this specific investigational peptide.

Read the Retatrutide Case Study

New here? Read in this order

If you're evaluating a COA or building a testing program for the first time, this sequence builds the full picture step by step.

1

Start with the overview

See why all four tests exist and how they fit together on the Peptide Testing hub page.

2

Learn purity

Understand chromatograms, purity grades, and what HPLC can and can't tell you in the HPLC guide.

3

Confirm identity

See why mass matching is required in the LC-MS guide — HPLC alone can't catch substitutions.

4

Verify injectable safety

Review sterility and endotoxin guidance together because the two methods evaluate different forms of contamination.

Quick glossary

Key terms that come up across every guide.

COACertificate of Analysis — the batch-specific document reporting all test results for a given lot.
ISO/IEC 17025The international accreditation standard for testing and calibration laboratories.
RP-HPLCReverse-Phase High-Performance Liquid Chromatography — the standard purity method for peptides.
ESIElectrospray Ionization — the standard ionization method used to generate peptide ions for LC-MS.
USP <71> / <85>United States Pharmacopeia chapters governing sterility testing and bacterial endotoxin testing, respectively.
EU (Endotoxin Unit)The standardized unit of endotoxin activity, calibrated against the U.S. Reference Standard Endotoxin.

Ready to request independent peptide testing?

Submit a sample for independent laboratory analysis and receive documentation based on the testing methods selected for your project.

Resource guide compiled from PeptideValidation.com's published testing standards. For educational and informational purposes only — not medical advice.