With over 30 years of strong foothold in the pharmaceutical industry, we take pride to be established as a quality oriented and customer centric manufacturer who understands the value of delivering quality products on time.

To ensure this world-class quality, we have independent QA and QC teams in each of our manufacturing facilities, working in tandem with each other and with the rest of the facility, adhering to current GMP practices.Our SAP based API manufacturing facility is US-FDA approvable, with strict adherence to USP, EP as well as IP standards. We have a dedicated regulatory affairs department to support the organization right from preparing technical packages for customer for initial assessment to preparing and filing dossiers with updated information from customers.

We constantly update our knowledge by conducting trainings across the organization on GMP standards, regulatory requirements and personality development, to ensure all-round development of our employees.