Certificates Of Analysis & Testing Documentation.
Every batch undergoes structured analytical validation including purity, identity, endotoxin screening, sterility testing, and heavy metal analysis — all documented in batch-specific Certificates of Analysis.
14x Testing
Multi-stage analytical verification system
Batch COA
Each product linked to unique reports
Third Party
Independent FDA-audited labs
Verified Data
Transparent analytical reporting
Certificate Of Analysis Explained.
A Certificate of Analysis (COA) is a batch-specific document that records the full laboratory test results for a product run. It confirms that each batch meets defined analytical specifications before release.
Our COAs include identity verification, purity analysis (HPLC), endotoxin testing (LAL), sterility testing (USP <71>), heavy metal screening (ICP-MS), and additional quality controls.
What Every Certificate Includes.
Purity (HPLC)
Measures compound concentration and related impurities.
Identity Testing
Confirms molecular structure matches reference standard.
Endotoxin Testing
Detects bacterial endotoxin contamination (LAL method).
Sterility (USP <71>)
Ensures no microbial contamination is present.
Heavy Metals
ICP-MS screening for trace elemental impurities.
Residual Solvents
GC-MS testing for manufacturing solvent residues.
Need A Specific Batch COA?
Each product includes a QR-linked Certificate of Analysis. Contact support if you need assistance locating a specific batch report.