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Third-Party HPLC Tested HPLC Tested
Third-Party Verification

Clinical Lab Reports
& HPLC Testing Data

Transparency is the foundation of clinical research. Every batch of Forged Pharma compounds undergoes rigorous, independent third-party analytical testing to guarantee absolute purity, precise concentration, and the absence of heavy metals or biological contaminants.

Standard

99%+ Purity

Methodology

HPLC-UV / MS

Filter Registry:
Testosterone Cypionate COA
Injectable Passed

Testosterone Cypionate

Batch Analysis & Concentration

Deca Durabolin COA
Injectable Passed

Deca Durabolin

Nandrolone Decanoate Analysis

BPC-157 COA
Peptide Passed

BPC-157 (10mg)

Lyophilized Peptide Purity

TB-500 COA
Peptide Passed

TB-500 (5mg)

Lyophilized Peptide Purity

HGH COA
Growth Hormone Passed

Somatropin (HGH)

100 IU Kit Verification

Anavar COA
Oral Tablet Passed

Anavar (Oxandrolone)

Tablet Concentration Analysis

Proviron COA
Oral Tablet Passed

Proviron (Mesterolone)

Tablet Concentration Analysis

Missing a Compound?

We routinely update our testing database. Contact support to request specific batch results.

Protocol Transparency

Analytical Methodology

We utilize industry-standard pharmacological testing protocols to ensure our researchers receive exactly what is on the label. Our multi-phase verification process leaves zero room for guesswork.

HPLC-UV Verification

High-Performance Liquid Chromatography separates the compound into its individual components. This allows us to verify the exact concentration (mg/ml) and ensure the active pharmaceutical ingredient (API) matches the label claim with >99% accuracy.

Mass Spectrometry (MS)

By measuring the mass-to-charge ratio of ions, Mass Spectrometry provides a definitive molecular fingerprint of the substance. This confirms the absolute identity of the compound, ensuring no substitutions or degradation has occurred.

Contaminant Screening

Beyond purity and concentration, our raw materials undergo strict screening for heavy metals (lead, arsenic, mercury) and microbial pathogens. All injectable carrier oils are further sterilized to pharmaceutical standards to prevent injection-site complications.

How to Read
Your C.O.A.

Understanding the data on our certificates guarantees confidence in your research protocol.

01.

Check the API

Verify the "Analyte" or "Compound Name" matches exactly what you ordered.

02.

Verify Purity %

Look at the chromatogram peak area. We require a minimum of 99% baseline purity.

03.

Concentration

For liquids/orals, ensure the tested mg/ml or mg/tab matches the label dosage claim.

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