Generics

We manufacture our products by following our customers’ and health authorities’ most stringent requirements. DMF documentation for all our products is prepared in accordance with the latest requirements 
of EDQM (CEP), ICH (ASMF in eCTD format), and FDA (US DMF). Material and product testing is performed in line with the European and United States Pharmacopeias.

We provide

professional supporting areas related to technology, analytical and special services.

We collaborate

closely with you in order to search for and suggest solutions on a day-to-day basis working in parallel with your technicians and analysts to offer the best solutions along the way.

We support

and help you to overcome challenges during your formulation development through solutions tailored to your needs.