Quality Control Department

Quality Control Department

The Quality Control Department is responsible for ensuring that pharmaceutical products, raw materials, and finished products comply with established quality standards. The Department evaluates the composition, purity, safety, and stability of products using modern physicochemical and instrumental analytical techniques.

In addition, the Department organizes laboratory testing, documents analytical results, and maintains all quality-related records and documentation.

The Department ensures compliance with the Quality Management System (QMS) as well as applicable national and international standards throughout the manufacturing process.

It also investigates identified non-conformities, develops corrective and preventive recommendations, and implements measures aimed at the continuous improvement of product quality.

Through these activities, the Department contributes to providing consumers with safe, effective, and high-quality pharmaceutical products.