The Quality Standard
Analytical data over marketing. Our protocols are designed to eliminate variables in your research.
Phase 01
Synthesis
We partner exclusively with ISO 9001:2015 certified synthesis laboratories. Each vendor undergoes qualification before any batch is accepted. Raw material documentation, synthesis reports, and chain-of-custody records are retained for every lot.
Phase 02
Sampling
Raw materials are quarantined upon arrival. Random samples are pulled from the batch in a sterile environment to ensure the test sample is truly representative of the entire lot. Sampling is performed under controlled conditions with full documentation prior to testing.
Phase 03
Independent Testing
Every batch is submitted to accredited third-party laboratories — including MZ Biolabs and Janoshik Analytical — for HPLC and Mass Spectrometry. These laboratories operate under ISO/IEC 17025 accreditation, the international standard for testing laboratory competence.
Phase 04
Certificate Issued
Only after third-party results confirm >99% purity is a lot released for fulfillment. The Certificate of Analysis is published directly to our library and the lot is made available for research. View COA Library →