Our Standards
Quality Assurance
Every compound we supply undergoes a rigorous multi-stage quality control process. Transparency and traceability are non-negotiable at Neogenesis BioLabs.
Our Process
From Synthesis to Shipment
Our QA pipeline is designed to ensure every vial that leaves our facility meets the highest standards for purity, stability, and documentation. Each step is independently verified and fully traceable.
Sourcing & Synthesis
All synthesis precursors are sourced from verified suppliers with documented purity certifications. Compounds are then synthesized via solid-phase peptide synthesis (SPPS) under controlled conditions, with each batch assigned a unique lot number for end-to-end traceability.
HPLC Purity Analysis
Every batch undergoes high-performance liquid chromatography (HPLC) analysis to verify purity. A minimum of ≥99% purity is required before any batch is approved for release.
Mass Spectrometry Verification
Mass spectrometry (MS) confirms the molecular weight and sequence identity of each compound, ruling out structural variants, impurities, or contaminants before proceeding to independent testing.
Third-Party US Lab Testing & COA
All compounds are independently verified by accredited US-based laboratories. A Certificate of Analysis (COA) is generated per batch — documenting purity, molecular weight, lot number, and methodology — and is available on request for all products.
Catalog Listing & Release
Only compounds that pass every stage of our QA process are approved for listing in our catalog. Batches that do not meet our purity and documentation standards are rejected and never made available for purchase. When you order from Neogenesis BioLabs, every product has already cleared our full verification pipeline.
Packaging & Fulfillment
Approved compounds are sealed under controlled conditions and stored at recommended temperatures (36°F–46°F) until shipment. Full lot traceability is maintained from synthesis through delivery.
≥99% Purity
Minimum purity threshold required for batch release via HPLC analysis.
COA Available
Full Certificate of Analysis available on request for every product batch.
US Third-Party Tested
Independent verification by accredited US-based laboratories on every batch.
Full Batch Documentation
Every batch is fully documented from synthesis to shipment with unique lot tracking.