Uncompromising Quality at Every Step
From raw material sourcing to final packaging, every batch undergoes rigorous quality control. Our ISO-certified processes ensure consistent purity and reliability for your research and manufacturing needs.
Industry-Leading Standards
Our facilities and processes are certified to meet the highest international quality standards.
ISO 9001:2015
Quality Management System certification ensuring consistent product quality and continuous improvement.
GMP Compliant
Manufacturing practices that meet Good Manufacturing Practice guidelines for pharmaceutical-grade products.
Clean Room
Class 100,000 clean room facilities for contamination-free peptide synthesis and packaging.
Third-Party Verified
Regular audits and independent testing verification to ensure ongoing compliance and accuracy.
Our QC Process
Every batch goes through a comprehensive 6-step quality control process before release.
Raw Material Inspection
All incoming amino acids and reagents are tested for purity and quality before entering the production process. Only materials meeting our strict specifications are approved.
In-Process Monitoring
During synthesis, we conduct real-time monitoring of coupling efficiency, temperature, and pH levels. Any deviation triggers immediate investigation and corrective action.
HPLC Purity Analysis
High-Performance Liquid Chromatography analysis confirms peptide purity. We guarantee minimum 98% purity, with most batches exceeding 99%.
Mass Spectrometry (MS)
LC-MS/MS analysis verifies molecular weight and confirms the identity of each peptide. This ensures you receive exactly what was ordered.
Endotoxin & Bioburden
For pharmaceutical applications, we perform endotoxin testing (LAL method) and bioburden analysis to ensure products meet sterility requirements.
Final Release & COA
QA Manager reviews all test results before batch release. A comprehensive Certificate of Analysis accompanies every shipment.
Advanced Analytical Equipment
State-of-the-art instruments ensure accurate and reliable quality testing.
HPLC Systems
High-performance liquid chromatography for precise purity analysis and impurity profiling.
LC-MS/MS
Liquid chromatography-mass spectrometry for molecular weight confirmation and identity verification.
Amino Acid Analyzer
Quantitative amino acid composition analysis to verify peptide content and sequence.
Karl Fischer Titrator
Precise water content determination to ensure proper moisture levels for stability.
Peptide Synthesizers
Automated solid-phase peptide synthesis for consistent, high-quality production.
Lyophilizers
Freeze-drying systems for stable, long-shelf-life peptide powder production.
Complete Batch Documentation
Every shipment includes comprehensive documentation for your records and regulatory compliance.
Certificate of Analysis (COA)
Detailed analytical report for each batch including all test results and specifications.
HPLC Chromatogram
Full chromatographic data showing peak purity and retention times for verification.
Mass Spectrum
MS data confirming molecular weight and structural identity of the peptide.
MSDS / SDS
Material Safety Data Sheets with handling, storage, and safety information.
Request Quality Documentation
Need COA samples or want to verify our quality standards? Contact us for documentation or to schedule a facility audit.