As a worldwide leading supplier, we emphasize the importance of offering quality products with the appropriate regulatory documentation. We are fully aware of the importance of the registration process phases for a drug within the pharmaceutical industry, which makes us the qualified partner when requiring Quats of cGMP pharmaceutical quality.

Our Quality system meets DS/EN ISO 9001 and ICH's cGMP Guide for Active Pharmaceutical Ingredients (ICH Q7). Uniform quality and safety of finished products is ensured by our efficient quality control systems, computerised materials planning and rigorous laboratory quality control. In-process samples, as well as finished products, are carefully analysed in our modern, well-equipped laboratory.

Our dedicated Environmental Department encourages the environmental consciousness of our staff, by ensuring that each member has the necessary skills and knowledge to minimise environmental impact while on the job. We have implemented an Environmental Policy, and are DS/EN ISO 14001 as well as OHSAS 18001 certified.