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

HPLC Analysis

High-Performance Liquid Chromatography measures purity levels to ≥99%, identifying impurities and degradation products with precision.

Mass Spectrometry

LC-MS/MS identifies molecular weight and structure, confirming product identity and detecting undeclared ingredients.

Sterility Testing

USP <71> bacterial and fungal sterility assays ensure injectables are safe and free from microbial contamination.

Endotoxin Testing

LAL testing confirms endotoxin levels below safe thresholds for injectable research compounds.

Water Content

Karl Fischer titration measures residual moisture, ensuring stability and shelf life.

Elemental Analysis

ICP-MS confirms elemental composition and detects heavy metal contaminants.

The COA Process

1
Sample Submission

Each batch is submitted to our ISO 17025-accredited partner lab with batch-specific identifying information.

2
Testing

Compounds undergo comprehensive multi-method analysis (HPLC, MS, sterility, endotoxin) as documented in our protocol.

3
Results Review

Results are analyzed, documented, and verified for accuracy and compliance with specifications.

4
QR-Linked COA

A unique QR code links to the batch-specific Certificate of Analysis, verifiable and traceable.

Quality Standards

ISO 17025 Accreditation — Labs meet international standards for competence and impartiality in testing.
≥99% Purity Threshold — All products must meet or exceed 99% purity by HPLC.
Batch-Specific Testing — Every batch is individually tested, never pooled or assumed.
Zero Undeclared Ingredients — Mass spectrometry confirms no hidden compounds or contaminants.
Traceable Documentation — QR codes link to detailed lab reports with signatures and accreditation proof.
Third-Party Only — No in-house testing. Complete independence from manufacturing and sales.