quality control

At Vakzine Pharma, our Quality Control function ensures that every product meets the highest standards of safety, purity, and efficacy. We follow stringent testing protocols, validated analytical methods, and rigorous documentation practices to ensure full compliance with national and international regulatory requirements. From raw materials to final product release, every stage undergoes systematic checks to guarantee consistency and reliability. 

We verify all incoming raw materials through identity, purity and quality checks before they enter production. During manufacturing, in-process samples are continuously monitored to ensure that each step meets defined specifications, preventing deviations and ensuring batch uniformity. 

We maintain consistent accuracy through regular calibration of analytical instruments and periodic performance checks. All testing methods are validated for precision, accuracy, specificity, and reproducibility, ensuring reliable and scientifically sound results every time. 

All QC operations follow strict Good Laboratory Practices (GLP) with emphasis on accuracy, traceability, and transparent reporting. Electronic records, audit trails, and standardized documentation systems help ensure complete data integrity and regulatory compliance. 

Our QC team conducts real-time and accelerated stability studies to evaluate product performance under various environmental conditions. These studies help determine shelf-life, storage requirements, and overall product integrity throughout its lifecycle. 

Every batch of finished product undergoes comprehensive analytical, physical, and microbiological testing. Our team ensures compliance with pharmacopeial standards and stability expectations before products are approved for market release.