Third-party verified • HPLC tested • USP standards

Lab Reports & Third-Party Testing

Every batch independently verified. No claims without proof.

🔬
HPLC + Mass Spec
Pharmaceutical-grade testing
USP Validated
Methods validated to USP standards
📋
Full COAs
Complete certificates of analysis

Certificates of Analysis

Download the complete lab report for each batch. Independently tested by certified laboratories.

VERIFIED

SEMA-1

Semaglutide Research Compound
Batch Number VCB-SEMA-2501
Purity (HPLC) >99.2%
Testing Date January 2025
Testing Lab Peptide Test (MI)
Download COA (PDF)
VERIFIED

TRZ-2

Tirzepatide Research Compound
Batch Number VCB-TRZ-2501
Purity (HPLC) >99.4%
Testing Date January 2025
Testing Lab Peptide Test (MI)
Download COA (PDF)
VERIFIED

RT-3

Retatrutide Research Compound
Batch Number VCB-RT-2501
Purity (HPLC) >99.1%
Testing Date January 2025
Testing Lab Peptide Test (MI)
Download COA (PDF)
COMING SOON

MOTS-C

Mitochondrial Research Peptide
Batch Number Testing in progress
Purity (HPLC) Pending
Expected February 2025
Testing Lab Peptide Test (MI)
COA Pending
COMING SOON

NAD+ 1000mg

Cellular Energy Coenzyme
Batch Number Testing in progress
Purity (HPLC) Pending
Expected February 2025
Testing Lab Peptide Test (MI)
COA Pending

Our Testing Process

How we verify every batch before it reaches you.

1

Sample Collection

Random samples pulled from each production batch and sealed for testing.

2

Third-Party Lab

Samples sent to independent HPLC testing facility with no affiliation to Velocell.

3

HPLC Analysis

High-performance liquid chromatography determines purity and identifies impurities.

4

Mass Spectrometry

Molecular weight confirmed via mass spec to verify compound identity.

5

COA Generation

Lab issues Certificate of Analysis with chromatogram, results, and signature.

6

Public Release

Full COA published here. Only batches meeting >99% purity are sold.

Testing Partner

Our compounds are tested by Peptide Test, an independent analytical laboratory in Michigan. Their methods are validated according to United States Pharmacopeia (USP) standards—the gold standard for pharmaceutical testing.

✓ ISO/IEC 17025 Standards • USP Validated Methods