For Research Use Only [email protected]

Certificates of Analysis

Third-party COA documentation available for every product upon request.

What a COA Verifies

A Certificate of Analysis (COA) is a document issued by an independent third-party laboratory that confirms the characteristics of a research compound batch. For each product, a COA verifies:

  • Purity percentage, confirmed by HPLC analysis
  • Compound identity and molecular weight confirmation
  • Physical appearance of the lyophilized or crystalline material
  • Sterility and batch information

Why It Matters for Research Integrity

Reliable research depends on knowing exactly what is in each vial. COA documentation gives researchers verifiable confirmation of purity and identity before any laboratory work begins, supporting reproducibility and data integrity. All Pepvela products are for laboratory research purposes only and are not for human consumption.

Third-Party Verified COAs

Independent third-party analysis for every batch. Request a COA for any product not yet listed.

Metabolic

Retatrutide 10mg

Certificate of Analysis -- Retatrutide 10mg

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Metabolic

Retatrutide 30mg

Certificate of Analysis -- Retatrutide 30mg

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Cognitive

Selank 10mg

Certificate of Analysis -- Selank 10mg

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Growth Hormone

CJC-1295 + Ipamorelin

Certificate of Analysis -- CJC-1295 + Ipamorelin Blend

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Tissue Repair

BPC-157

Certificate of Analysis -- BPC-157 (Janoshik Task #148112)

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Tissue Repair

TB-500

Certificate of Analysis -- TB-500 (Janoshik Task #148111)

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Longevity

GHK-Cu 50mg

Certificate of Analysis -- GHK-Cu 50mg

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Longevity

Epitalon 10mg

Certificate of Analysis -- Epitalon 10mg

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Longevity

MOTS-c 10mg

Certificate of Analysis -- MOTS-c 10mg

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Testing and Quality Standards

Independent third-party testing for purity, identity, and quality assurance.

Our Testing Process

Every research compound batch undergoes high-performance liquid chromatography (HPLC) analysis performed by independent third-party laboratories. This process separates and quantifies the components of a sample, allowing precise verification of purity and identity before a batch is made available for research inquiry.

Testing is conducted per batch, so documentation always reflects the specific lot being supplied.

What Is Tested

Each batch is evaluated across the following parameters:

  • Purity percentage (98%+ target, confirmed by HPLC)
  • Compound identity and molecular weight confirmation
  • Physical appearance of the material
  • Sterility and batch consistency
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