About Our Manufacturing Facility
Our pharmaceutical manufacturing facility is designed to meet global standards with a focus on product safety, efficiency, and regulatory compliance. We maintain controlled environments, follow validated SOPs, and ensure end-to-end traceability from raw material sourcing to final dispatch. The facility supports scalable production for domestic and international markets with export-oriented infrastructure. Each section — including production, quality control, packaging, and warehousing — is strategically planned to maximize hygiene, reduce contamination risk, and enhance productivity. Advanced machinery and trained personnel ensure consistent quality across every product line.
Cleanroom & Hygienic Environment
Our facility maintains pharmaceutical-grade hygiene through advanced HVAC systems, HEPA filtration, positive pressure zones and strict environmental monitoring. Every process is executed under SOP-based guidelines to ensure product safety and zero contamination. Personnel undergo trained gowning procedures before entering classified areas. Environmental parameters such as temperature, humidity and microbial levels are continuously tracked. Airlocks are used to prevent cross-contamination and material movement is fully controlled with barcode tracking. Dedicated personnel monitor and validate cleaning protocols regularly.
- Class 100 (ISO 5) test-mutted small*
- Class 10,000 / ISO 7 zones for non-sterile production
- ISO 5 local zones for aseptic operations (where applicable)
- Regular microbiological monitoring & validation
