WHO-GMP Compliant cGMP Standards | CIN: U46491UT2026PTC021043 GSTIN: 05AAPCR6291N1ZK
UPSIDC Selaqui, Dehradun, Uttarakhand | Partner Inquiry
NUTRACEUTICAL & FOOD PRODUCT PORTFOLIO
Quality Assurance & Total Quality Management

Total Quality Management: Zero-Defect Pharmaceutical Precision

Bridging the nutraceutical quality gap through end-to-end analytical rigor, validated cleanroom environments, and cGMP compliance in Selaqui, Dehradun.

Zero Compromise Standard

Building Quality Into Every Formulation

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.

Quality Assurance & Testing at Ranjauly Health Care
Zero-Defect Goal
100% IPQC Inspection
Class 100,000
HEPA Filtered Cleanrooms
Multi-Barrier Quality Framework

The 4 Pillars of Our TQM Architecture

Our Total Quality Management program operates across every touchpoint from vendor qualifications and raw material arrival to packaging line release.

01
Stage 01
Inbound RM

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.

02
Stage 02
In-Process Quality Control (IPQC)

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.

03
Stage 03
Cleanroom & Environmental Controls

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.

04
Stage 04
Finished Batch Release & Stability Profiling

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.

Transparency & Compliance

Schedule a Facility Quality Audit