The Lab Standards
Our commitment to quality is not a marketing claim — it is an operational standard built into every step of our manufacturing process.
Where Purity
Meets Precision
EliteGen Labs is the only company in our industry offering US-compounded research peptides manufactured in a lab that follows cGMP (Current Good Manufacturing Practices) protocols. This distinction is not incidental — it is the foundation of everything we do.
cGMP certification means our facility, processes, personnel, and documentation all meet the rigorous standards set by the FDA for pharmaceutical manufacturing. While our products are for research use only, we hold ourselves to the same quality standards as the pharmaceutical industry.
The result is a product that researchers can trust: consistent, pure, stable, and fully documented from raw material to final vial.
cGMP Compliant Facility
Current Good Manufacturing Practices
FDA-Registered Suppliers
All raw material sources are FDA-registered
≥99% Purity Standard
Verified by independent HPLC-MS analysis
Batch-Level CoA
Certificate of Analysis for every production batch
From Synthesis to Your Laboratory
Raw Material Sourcing
We source exclusively from FDA-registered suppliers whose manufacturing sites are registered with the U.S. FDA. Every raw material arrives with a Certificate of Analysis before entering our facility.
Solid-Phase Peptide Synthesis
Our peptides are synthesized using advanced Solid-Phase Peptide Synthesis (SPPS) — the gold standard for producing high-purity, research-grade peptide sequences with precise control over the amino acid chain.
HPLC Purification
Post-synthesis, every compound undergoes multi-stage High-Performance Liquid Chromatography (HPLC) purification to remove impurities and achieve purity levels exceeding 99%.
Third-Party Verification
Before any product ships, it is sent to an independent, accredited third-party laboratory for HPLC-MS analysis. The resulting Certificate of Analysis is available for every batch.
Lyophilization & Packaging
Verified compounds are lyophilized (freeze-dried) for maximum stability and shelf life, then packaged in a controlled environment under cGMP protocols to prevent contamination.
Quality Release
Only batches that pass all internal and third-party quality checks are released for sale. Any batch that does not meet our standards is rejected — no exceptions.
Our Non-Negotiable
Standards
cGMP Compliant Facility
Current Good Manufacturing Practices
FDA-Registered Suppliers
All raw material sources are FDA-registered
≥99% Purity Standard
Verified by independent HPLC-MS analysis
Batch-Level CoA
Certificate of Analysis for every production batch
Lyophilized Stability
Freeze-dried for maximum shelf life and potency
US-Based Manufacturing
100% compounded in the United States
Solid-Phase Synthesis
Advanced SPPS methodology for precision
Independent Testing
Third-party accredited laboratory verification
