Automated Manufacturing Infrastructure
Operating 4 WHO-GMP certified manufacturing units engineered with robotic automation and ISO Class 5 sterile isolators.
State-of-the-Art Pharmaceutical Plant Architecture
Our manufacturing facilities are built according to global cGMP standards. Features include terminal HEPA filtration (0.3 micron 99.997%), differential cleanroom pressure zoning, and zero-dead-leg purified water loops (WFI).
5B+
Tablets & Capsules / Year200M
Aseptic Injectables / YearFacility Highlights
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Blow-Fill-Seal (BFS) TechnologyContainer forming, filling, and sealing in a 3-second continuous sterile cycle.
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Lyophilization CapacityIndustrial freeze-drying units with automatic vial loading and stoppering under vacuum.
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Automated Vision InspectionHigh-speed camera particle inspection system ensuring 100% defect-free output.
6-Step Quality Manufacturing Process
Raw Material Sampling & QC
100% identity verification of APIs and excipients using NIR spectroscopy in ISO Class 7 sampling booths.
Fluid Bed Granulation
High-shear mixer granulators and closed-system fluid bed processing ensuring uniform granule density.
High-Speed Tableting
Automated double-sided rotary presses with automatic weight control and inline hardness monitoring.
Aseptic Liquid Filling
Sterile filling under ISO Class 5 laminar air flow isolators with continuous particle counting.
Alu-Alu Blister Packaging
Cold-formed aluminum foil sealing ensuring maximum moisture barrier protection for global exports.
GS1 Serialization & QA Release
2D DataMatrix track & trace serialization per carton before final Quality Assurance batch certificate release.