Quality isn't a stage. It's culture.
From raw material intake to final release, every batch passes through six quality gates and dozens of instrumented checks.
Independently verified.
Continuously audited.
WHO-GMP
World Health Organization Good Manufacturing Practices certified for all active lines.
ISO 9001:2015
Quality Management System certified for consistent product and service provision.
ISO 14001
Environmental Management System certified for sustainable operations.
Schedule M
Compliant with Indian Drugs and Cosmetics Act manufacturing protocols.
FSSAI
Food Safety and Standards Authority of India certified for neutraceuticals.
CDSCO
Central Drugs Standard Control Organization approved.
Every batch. Every time.
Raw material inspection
Every incoming API and excipient is quarantined and tested before entering the floor.
In-process monitoring
Continuous checks on weight, thickness, hardness, and friability during compression.
Analytical testing
HPLC, GC, and spectrophotometric analysis to confirm assay and purity profiles.
Stability studies
Accelerated and real-time stability chambers ensure shelf-life efficacy.
Batch release
Final QA review of all batch manufacturing records before market authorization.
Retention samples
Samples from every batch are retained in controlled conditions for future reference.