Search any released batch by compound or lot number. Every certificate below is the actual signed COA for that lot, issued by our manufacturing partner and linked as a downloadable PDF.
Pick from the index · swipe or use ‹ › / arrow keys · download the signed PDF
How our manufacturing partner builds, tests, and releases each lot. Summarized from NuLumin Bio-Sciences standards documents (Manufacturing Standards DOC-MFG-001 Rev 04; Research Standards, QMS owner M. Lavoie).
US-based solid-phase peptide synthesis (SPPS) at a cGMP-aligned, ISO-9001 facility (Noble Harbor, California), with quality systems audited per ICH Q7. Each peptide is assembled one residue at a time, then cleaved and purified.
Every batch is held to a ≥98% purity minimum, confirmed by reverse-phase HPLC and mass spectrometry. Independent third-party analysis (pH Solutions) covers microbials, mycotoxins, water activity, residual solvents, and heavy metals.
A documented paper trail follows every lot — synthesis, cleavage, purification, HPLC and MS results, lyophilization, and COA generation — retained from raw-material receipt through shipping and retrievable by lot number alone.
Documentation reproduced from supplier materials for transparency. For Research Use Only · Not for Human Consumption.