Quality control

The quality control at Cardiaan is a meticulous and crucial process that ensures the products are safe, effective, and consistent. It involves a series of systematic checks and balances throughout the process, right from product sourcing to delivery. The primary goal is to prevent contamination, errors, and deviations that could compromise the efficacy and safety of the drugs.

The first step of our quality control starts with the selection of high-quality raw materials, which are subjected to rigorous testing to verify their identity, strength, quality, and purity. Cardiaan Life Sciences sources all its materials from one of the best pharmaceutical manufacturing company in India and one of the biggest exporter to the International market, Swiss Garnier. A stringent follower of GMP (Good Manufacturing Practices) by WHO, Swiss Garnier ensures all its raw material and products are extremely safe with precise formulations. Some of the big pharmaceutical companies across the globe source their materials from this same company.

At Cardiaan Life Sciences, paramount importance is given to maintaining a clean and controlled environment, with proper documentation, and rigorous training of personnel to ensure zero defect and deviation from the expected result. All of this while keeping in mind the cost effectiveness and credibility of the final products. In-process controls are conducted at various stages to verify that the drug is according to the established specifications. This may involve testing samples for physical, chemical, and microbiological attributes, as well as monitoring critical equipment and environmental conditions. Upon completion, the final product undergoes a thorough series of tests to confirm its identity, strength, quality, and purity. This includes assessing factors such as potency, dissolution, and stability. If any discrepancies are found, the product may be rejected, and the process may need to be repeated or adjusted.

A robust quality control system also includes a strong quality assurance component, which involves regular audits and reviews of the entire storage plant. This helps to identify potential areas for improvement and ensures that the company is continually refining its quality control procedures. A combination of stringent testing, adherence to GMP guidelines, in-process controls, and ongoing quality assurance is done to guarantee high-quality pharmaceuticals that meet regulatory standards and ultimately benefit patients.