We have a modern and well-equipped Quality Control (QC) laboratory, which ensures that our products are pure, safe, effective and are released only after thorough stage inspection as per stringent specifications, methods and procedures laid down by international guidelines viz. WHO-GMP and Schedule-M. We have also been accredited with ISO 9001:2015 etc. Our QC department has all necessary instruments for analysis of API, finished products, packaging and related materials used.

The control of the active pharmaceutical ingredients, other compounds and packaging includes activities for control of their physical and chemical properties and microbiological characteristics in accordance with the internationally recognized standards.

The products are monitored in all the phases of their manufacturing, with all their specifics Carefully monitored, until the final product is delivered which, from the aspect of physical, chemical and pharmaceutically-technological properties are completes appropriate The analytical methods used for the analysis are continuously upgraded and modernized and accordingly validated resulting in highest level of safety and confidence of their performances.

• 1. We encourage skill development through learning, leadership and mentoring.
• 2. We employ motivated and committed people.
• 3. We measure performance and strive for continual improvement, seeking better ways to do business
• 4. We select products and business partners that conform to the highest international standards
• 5. RM/PM analysis (Flowchart)
• 6. Finished Products analysis (Flowchart)
• 7. In-process Checks (Flowchart)
• 8. Stability Studies