Our manufacturing processes are based on Six Sigma & Lean principles, aiming to eliminate and minimize waste. This approach increases the value-added to our products and services while preserving and protecting the environment by reducing waste and energy consumption.

Yes, our facilities have been audited by the FDA and are cGMP (Current Good Manufacturing Practices) compliant. This ensures that our production and filling line operations meet the highest standards set by regulatory authorities.

Yes, we have undergone regular FDA audits and adhere to GMP (Good Manufacturing Practices).

Absolutely. Our facility is equipped with high-capacity bulk processing and storage capabilities, allowing us to efficiently manage both OTC (Over The Counter) and non-OTC products with a range of compounding and filling operations tailored to meet diverse needs.

Our compounding capacities include various sizes of jacketed and non-jacketed kettles, compliant with OTC standards, capable of handling a wide range of volumes. For filling operations, we have equipment that can fill tubes, liquids, and bulk products, ranging from small bottles to tanker loads, adhering to OTC compliance.

We ensure product quality and consistency through outstanding process control and variation management, defect reduction, advanced quality management systems, and continuous quality improvement practices. Our commitment to improved process stability is reflected in our rigorous manufacturing statistical analysis.