Analytical Laboratory

Empirical testing for global compliance

In-house chromatographic and microbiological assay suites quantify active biomarkers, screen heavy metals, and confirm ingredient identity across every production batch.

Assay Benchmarks

Quantified verification thresholds

<0.1 ppm

heavy metal detection floor

100%

incoming lot identity testing

3 Zone

climatic stability testing

24 Hr

COA turnaround on pilot batches

Three-Stage Control

Raw lot to finished release

Analytical verification starts before material enters blending. Raw botanicals, vitamins, and active isolates undergo FTIR spectroscopy and HPLC chromatography to verify purity monographs and eliminate adulteration risks.

Finished dosage units undergo dissolution testing, microbial pathogen plating, and accelerated environmental stress testing to substantiate shelf-life claims in target export jurisdictions.

Review standardized batch dossiers

Obtain unredacted laboratory certificates of analysis, test method summaries, and stability study templates for technical due diligence.