Third-Party Lab Testing
Every batch independently verified by ISO 17025-accredited laboratories. No internal testing. No exceptions. Complete transparency through batch-specific Certificates of Analysis.
Our Testing Methods
High-Performance Liquid Chromatography measures purity levels to ≥99%, identifying impurities and degradation products with precision.
LC-MS/MS identifies molecular weight and structure, confirming product identity and detecting undeclared ingredients.
USP <71> bacterial and fungal sterility assays ensure injectables are safe and free from microbial contamination.
LAL testing confirms endotoxin levels below safe thresholds for injectable research compounds.
Karl Fischer titration measures residual moisture, ensuring stability and shelf life.
ICP-MS confirms elemental composition and detects heavy metal contaminants.
The COA Process
Each batch is submitted to our ISO 17025-accredited partner lab with batch-specific identifying information.
Compounds undergo comprehensive multi-method analysis (HPLC, MS, sterility, endotoxin) as documented in our protocol.
Results are analyzed, documented, and verified for accuracy and compliance with specifications.
A unique QR code links to the batch-specific Certificate of Analysis, verifiable and traceable.