Disto Pharmaceuticals Pvt

We develop a range of semi-finished formulations in our ISO 9001, ISO 14001, GMP and WHO-GMP approved manufacturing facilities. The company’s forte is the customized development and manufacture of modified release pellets of various Active Pharmaceutical Ingredients (APIs) including different combination or blends in “Ready-To-Fill” form. Our development and manufacturing abilities are wide ranging and designed to meet customers’ expectations and stringent international regulations. Our team of qualified and experienced technical personnel, well equipped manufacturing facility, stringent quality control, documentation system conforming to cGMP and WHO-GMP requirements, have been instrumental in maintaining our premium position in this segment of the Indian pharmaceutical industry. We have serviced clients across 18 countries since inception in the following regions viz., MENA, CIS, South & South-East Asia and Latin America.