Our advanced facility supports scalable, flexible production for a wide range of pharmaceutical dosage forms. We manufacture both generic and proprietary preparations for human use, ensuring batch-to-batch consistency and regulatory compliance.
Core Elements of Our QMS:
- Four-tier documentation system (Policy; SOPs; Protocols; Records)
- Robust Quality Control Labs: Wet Lab; Instrumentation; Stability Chambers; Microbiology
- Continuous temperature; humidity & pressure monitoring with alert systems
- QA-led oversight for deviations; CAPA; product release; and change control
- Market complaint handling; periodic reviews; and regulatory audit readiness
- Training and audit systems embedded in organizational culture