• At Aaven Pharmaceutical Pvt Ltd, our Quality Control (QC) department is equipped with state-of-the-art technology to evaluate Active Pharmaceutical Ingredients (API), excipients, finished products, packaging, and associated materials.
Our Infrastructure
We pride ourselves on having a cutting-edge Quality Control laboratory designed to ensure that all our products are 100% pure, effective, and safe. Before launching any product into the market, we conduct a comprehensive evaluation in accordance with rigorous standards, techniques, and procedures aligned with international guidelines, including PIC/S and WHO-cGMP.
Our QC laboratory is one of the few in the industry to have achieved NABL accreditation, underscoring our commitment to maintaining high-quality standards. Aaven Pharmaceutical Pvt Ltd is proud to be a pioneer in the Indian pharmaceutical industry, compliant with international Good Laboratory Practice (GLP) criteria.
Key Activities of the Quality Control Department
- Analysis Through Flowcharts: We utilize flowcharts to outline and streamline our analysis processes, ensuring clarity and efficiency.
- Finished Product Analysis: Every finished product undergoes thorough testing to ensure it meets quality standards and specifications.
- Work-in-Progress Quality Checks: We conduct quality checks during the manufacturing process to identify and address any issues early on.
- Analysis of QC Lab and Instruments: Our laboratory instruments are regularly calibrated and maintained to guarantee accurate results.
- Waste Management: We implement effective waste management practices to ensure environmental compliance and sustainability.
- Wet Analysis Laboratory Management: Our wet analysis laboratory conducts critical testing for various parameters, contributing to the overall quality assurance.
- Microbiological Testing and Packaging QA Checks: We perform rigorous microbiological testing and quality assurance checks on packaging materials to ensure product safety and integrity.