Quality Assurance
At our pharmaceutical manufacturing facility, quality is the cornerstone of everything we do. We operate under a robust and well-documented Quality Management System (QMS) designed to ensure consistent production of safe, effective, and high-quality products.
Our operations strictly comply with the requirements of the Revised Schedule M guidelines, with infrastructure and systems aligned to WHO Good Manufacturing Practices (WHO-GMP) standards. Every stage of manufacturing—from raw material procurement to final product release—is governed by stringent quality controls and risk-based approaches.
Our Quality Assurance team ensures:
- Thorough review and approval of batch manufacturing and packaging records
- Compliance with validated processes and analytical methods
- Effective deviation, change control, and CAPA systems
- Continuous monitoring through internal audits and quality reviews
- Data integrity in line with ALCOA++ principles
We are committed to continuous improvement, regulatory compliance, and delivering products that consistently meet customer expectations and global quality standards.
QC Laboratories
Our QC labs are equipped to handle chemical, instrumental, and microbiological testing.
Chemical & Instrumental Lab
- HPLC
- UV Spectrophotometer
- FTIR
- Dissolution apparatus
- Stability chambers
Microbiology Lab
- Sterility (if applicable)
- Environmental monitoring
- Microbial limit testing
- Water testing
- Pathogen testing
Stability Studies
Stability testing is conducted as per ICH guidelines using controlled stability chambers.
