Bridging the nutraceutical quality gap through end-to-end analytical rigor, validated cleanroom environments, and cGMP compliance in Selaqui, Dehradun.
In modern nutraceutical manufacturing, quality cannot be merely inspected into a finished product it must be engineered into every single phase of the process. While the Indian nutraceutical market is expanding rapidly, the greatest industry challenge remains the absence of standardized quality norms, erratic testing, and reliance on unorganized players.
Ranjauly Health Care solves this challenge by instituting pharmaceutical-grade Total Quality Management (TQM). From segregated quarantine rooms for raw granules and tablets to positive-pressure Class 100,000 cleanrooms, Atlas Copco filtered oil-free compressed air, and continuous conductivity USP-grade purified water, every batch produced at our Selaqui facility complies with strict WHO-GMP benchmarks.
Our Total Quality Management program operates across every touchpoint from vendor qualifications and raw material arrival to packaging line release.
Every active ingredient, botanical extract, excipient, and primary packaging material undergoes analytical identity verification, assay testing, microbiological limits evaluation, and heavy metal screening before warehouse release.
Continuous on-floor testing during batch manufacturing: Loss on Drying (LOD) in FBD granules, tablet weight variation, hardness, thickness, and friability checks every 15�30 minutes, and softgel seam seal integrity.
Class 100,000 cleanrooms equipped with terminal HEPA filtration, positive pressure AHUs, Floor Differential Ventilation (FDV), and industrial dehumidifiers maintaining strict temperature and particle containment.
Comprehensive dissolution profiling, assay quantification, and real-time and accelerated stability chamber testing (Zone IVb: 40�C / 75% RH) ensuring formulation integrity across its entire shelf life.