Our quality policy is - Uncompromised focus towards control and consistency of quality products to keep up with the international standards of product manufacture and treatment.

The processes are well-managed with the help of a qualified team empowered with essential and necessary infrastructure, and technological support.

We have a well defined Quality Control & Quality Assurance Department managed by highly specialised & qualified technical staff which ensures that all the products are manufactured as per the international quality standards, and are released for sales into the market after they pass all stringent tests as per Drugs & Cosmetic Act, 1940. Quality Control Department has an excellent team of professionals having good understanding of concepts of quality systems and GLP.

Active Pharmaceutical Ingredients (API) and dosage forms are tested for specified parameters before release. Analytical testing is carried out with highly sophisticated instruments viz. HPLC, FTIR, UV spectrophotometer etc.

All the analytical test procedures and manufacturing procedures are well documented, and revision is undertaken as per specified protocol. Analytical methods are validated to give the reproducible results.

Manufacturing processes strictly adhere and comply with the norms, technical standards and statutory requirements, realising the importance of the requirements.