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.
Hover seal cards for 3D perspective depth or click to flip 180° for official license IDs and audit scope.
WHO-GMP
World Health Organization & FDA Maharashtra
World Health Organization Good Manufacturing Practices certified for all active lines.
WHO-GMP
WHO-GMP/MH/2026/894
World Health Organization & FDA Maharashtra
Sterile Parenterals, Euro-Head IV Lines & Oral Solids
Continuous environmental particle count, HEPA ISO Class 5/7 cleanrooms, and 100% batch release validation.
ISO 9001:2015
TÜV SÜD South Asia & ISO
Quality Management System certified for consistent product and service provision.
ISO 9001:2015
ISO/QMS/9001/2025-09
TÜV SÜD South Asia & ISO
Formulation R&D, QC Labs & Manufacturing
Continuous environmental particle count, HEPA ISO Class 5/7 cleanrooms, and 100% batch release validation.
ISO 14001
Bureau Veritas Certification
Environmental Management System certified for sustainable operations.
ISO 14001
ISO/EMS/14001/2025-11
Bureau Veritas Certification
Zero-Liquid-Discharge & Eco Plant Operations
Continuous environmental particle count, HEPA ISO Class 5/7 cleanrooms, and 100% batch release validation.
Schedule M
Food & Drug Administration Maharashtra
Compliant with Indian Drugs and Cosmetics Act manufacturing protocols.
Schedule M
SCH-M/2841/MUM
Food & Drug Administration Maharashtra
Schedule M Parenteral & Solid Dosage Lines
Continuous environmental particle count, HEPA ISO Class 5/7 cleanrooms, and 100% batch release validation.
FSSAI
FSSAI Government of India
Food Safety and Standards Authority of India certified for nutraceuticals.
FSSAI
FSSAI/10020022011942
FSSAI Government of India
Nutraceutical Syrups, Softgels & Oral Liquids
Continuous environmental particle count, HEPA ISO Class 5/7 cleanrooms, and 100% batch release validation.
CDSCO
CDSCO Ministry of Health & Family Welfare
Central Drugs Standard Control Organization approved.
CDSCO
CDSCO/MFG/WZ/2025/1102
CDSCO Ministry of Health & Family Welfare
National Wholesale Manufacturing License
Continuous environmental particle count, HEPA ISO Class 5/7 cleanrooms, and 100% batch release validation.
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.