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Quality Assurance

Third-Party Verified.
Every Batch. Every Time.

We don't ask you to trust us blindly. Every PEPTARA Health product is independently tested by a certified laboratory, with documentation available on request.

>99% Purity Standard
HPLC + Mass Spec Testing
Independent 3rd-Party Labs
COA on Every Batch
Our Process

How We Verify Every Product

Our quality assurance process is designed to eliminate uncertainty at every step — from synthesis to your lab.

1

GMP Synthesis

All peptides are synthesised at GMP-certified facilities using solid-phase peptide synthesis (SPPS) under controlled conditions.

2

Internal QC Check

Before submission to third-party testing, each batch undergoes an initial quality control review at the synthesis facility.

3

Independent Lab Testing

Samples are submitted to a certified, independent third-party laboratory for HPLC and mass spectrometry analysis.

4

COA Issued & Shipped

Only batches that meet our >99% purity threshold receive a COA and are approved for inventory and shipment.

Testing Methods

What We Test For

Our testing protocols are designed to verify every critical quality parameter for research-grade peptides.

HPLC Purity Analysis

High-Performance Liquid Chromatography (HPLC) is used to measure the purity percentage of each compound, ensuring all products meet our minimum >99% threshold.

Mass Spectrometry

Mass spectrometry confirms the molecular weight and identity of each peptide, verifying that the correct compound has been synthesised with the expected structure.

Sterility Testing

Select products undergo sterility testing to confirm the absence of microbial contamination, critical for maintaining the integrity of lyophilised research compounds.

Moisture Content

Water content analysis ensures that peptide powders meet required moisture specifications for long-term stability during storage and shipping.

Amino Acid Analysis

For complex peptides, amino acid composition analysis confirms that the sequence and ratio of amino acids matches the expected molecular profile exactly.

Residual Solvent Testing

Residual solvent levels are tested to ensure compounds are free from synthesis byproducts or organic solvents that could compromise research results.

Request a COA

Get Your Certificate
of Analysis

COA documents are available for every product and batch. Fill in the form or contact us directly.

What's in a COA?

A Certificate of Analysis from an independent laboratory provides verified documentation for your research records.

  • Product name and batch number
  • HPLC purity percentage
  • Mass spectrometry confirmation
  • Molecular weight verification
  • Testing laboratory details and accreditation
  • Test date and expiry recommendation
  • Pass/fail determination against our standards
Prefer to call?
(704) 605-9477
Text or call with your batch number

Request a COA

Provide your order details and we'll send the relevant certificate within 1 business day.

✅ COA request received. We'll email your certificate within 1 business day. For urgent requests, text (704) 605-9477.

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