Automated Manufacturing Infrastructure

Operating 4 WHO-GMP certified manufacturing units engineered with robotic automation and ISO Class 5 sterile isolators.

SCADA Industry 4.0 Integration

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 / Year

200M

Aseptic Injectables / Year

Facility Highlights

  • Blow-Fill-Seal (BFS) Technology
    Container forming, filling, and sealing in a 3-second continuous sterile cycle.
  • Lyophilization Capacity
    Industrial freeze-drying units with automatic vial loading and stoppering under vacuum.
  • Automated Vision Inspection
    High-speed camera particle inspection system ensuring 100% defect-free output.
Inline Control

6-Step Quality Manufacturing Process

01

Raw Material Sampling & QC

100% identity verification of APIs and excipients using NIR spectroscopy in ISO Class 7 sampling booths.

02

Fluid Bed Granulation

High-shear mixer granulators and closed-system fluid bed processing ensuring uniform granule density.

03

High-Speed Tableting

Automated double-sided rotary presses with automatic weight control and inline hardness monitoring.

04

Aseptic Liquid Filling

Sterile filling under ISO Class 5 laminar air flow isolators with continuous particle counting.

05

Alu-Alu Blister Packaging

Cold-formed aluminum foil sealing ensuring maximum moisture barrier protection for global exports.

06

GS1 Serialization & QA Release

2D DataMatrix track & trace serialization per carton before final Quality Assurance batch certificate release.