Scientific Integrity

Analytical Chemistry & Quality Verification

We verify botanical identity, standardize active marker yields, and eliminate impurities to deliver clinical-grade formulations with total transparency.

Three-Tier Quality Screening Matrix

Every single batch of botanical raw materials and finished formulations undergoes systematic validation at our ISO/GMP laboratory hubs.

Tier 01

HPTLC Identity Fingerprinting

High-Performance Thin-Layer Chromatography verifies exact plant genus and species.

Traditional visual identification is insufficient to detect species dilution or substitution. We utilize HPTLC fingerprinting to map the unique phytochemical signature of each plant against verified reference standards (USP/AHP), ensuring absolute authenticity before any crop is processed.

Tier 02

HPLC/UPLC Active Standardization

High-Performance Liquid Chromatography quantifies active phytochemical marker levels.

Consistent clinical potency requires standardized active compound percentages. We run quantitative HPLC or UPLC-MS assays on every batch. For example, our KSM-66® Ashwagandha is verified to contain ≥ 5% withanolides, and our Turmeric is standardized to 95% total Curcuminoids.

Tier 03

ICP-MS & GC-MS/MS Contaminant Screening

Inductively Coupled Plasma Mass Spectrometry monitors safety limits in parts-per-billion.

We screen for impurities to ensure clean, regulatory-compliant supply lines. ICP-MS checks for toxic heavy metals (Lead, Mercury, Cadmium, Arsenic). High-resolution Gas and Liquid Chromatography coupled with tandem mass spectrometry (GC-MS/MS & LC-MS/MS) screens for over 450 agricultural pesticide residues, solvent residues, and USP microbiological pathogens.

Analytical Compliance Limits

All wholesale batches are shipped with a batch-specific Certificate of Analysis (CoA) confirming the following testing standards:

Testing Parameter Methodology Wholesale Acceptance Limit Safety Target
Heavy Metals (Pb, Cd, As, Hg) ICP-MS Lead < 0.5 ppm, Cadmium < 0.2 ppm USP < 561 Compliant
Pesticide Residues GC-MS/MS / LC-MS/MS Non-Detectable (ND) EPA / EU Regulatory limits
Microbiological Count USP / AOAC Yeast/Mold < 100 CFU/g, E.coli/Salmonella Neg USP < 2021 Safe Limits
Phytochemical Markers HPLC / UPLC-MS Batch-specific (e.g., Withanolides ≥ 5%) Clinical Efficacy Guarantee
Solvent Residues Headspace GC-MS Non-Detectable (ND) for Hexane/Methanol Clean Label, CO2/Water only

Request Batch-Specific Technical Sheets

Are you a brand formulator or quality assurance manager seeking raw ingredient specifications, material safety datasheets (SDS), or HPTLC chromatogram profiles? Contact our scientific affairs office.

Contact Lab Director