Quality Assurance is integrated into every stage of our operations, from vendor qualification and raw material sourcing to manufacturing, packaging, and final product release. Our QA team works independently and oversees all systems to maintain global compliance and continuous improvement.
The company’s commitment to excellence goes beyond basic business and legal requirements. We work to deliver healthcare products that meet both national and international regulatory criteria.
Key QA Functions
1. Robust Documentation & Compliance
- Implementation of WHO-GMP standards
- Detailed Standard Operating Procedures (SOPs) for all activities
- Strict adherence to documentation practices ensuring traceability and transparency
2. Vendor & Raw Material Control
- Rigorous supplier qualification procedures
- Comprehensive testing of all raw materials, excipients, and packaging components
- Approval only after meeting predefined quality specifications
3. In-Process Quality Checks
- Continuous monitoring of critical parameters during manufacturing
- Line clearance procedures to prevent cross-contamination
- Real-time sampling and analysis to ensure consistency and accuracy
4. Finished Product Testing
All finished goods undergo extensive physical, chemical, and microbiological testing before release. Only batches that meet all regulatory and internal quality criteria are approved for dispatch.
Advanced Quality Infrastructure
Our QA operations are supported by a dedicated Quality Control laboratory equipped with:
- HPLC, UV and other analytical instruments
- Microbiology labs for sterility and contamination checks
- Stability chambers for accelerated and real-time stability studies
- Validated testing methods and calibration systems