Our state-of-the-art QC and Microbiology laboratory, a GLP Certified facility, is equipped with multiple HPLC systems with auto samplers, Gas Chromatography (GC), FTIR, UV Spectrophotometers, dissolution testers, TOC analyzer, stability chambers, and laminar airflow systems enabling high-precision analysis across raw materials, in-process stages, and finished formulations.
Aligned with Schedule M, GMP, WHO guidelines, and GLP principles, our QC framework is built on data integrity, traceability, and continuous improvement—making quality a definitive strength across all markets we serve.
We exercise stringent control at every step, from material receipt to final batch release, ensuring consistency and strict adherence to pharmacopeial standards. We drive quality excellence through advanced analytical capabilities and uncompromising regulatory compliance.