Intro Bio Pharma Inc. has been accelerating the development of new dosage form as well as improved new medicine based on the R&D technology and medicine production as a global partner of technological development of medicine dosage form since it was established in 2007.
Since January 2016, after Food & Drug Administration’s PIC/S GMP authorization, we have been making a new leap forward as a service company that is capable of production, quality control, and authorization apart from technical transfer. We are now transforming to the company that can handle both development and production.
Moreover, we are now providing solutions for development of clinically testing drug, production, and quality control based on the plentiful R&D experiences and PIC/S GMP facility so that pharmaceuticals and bio ventures that do not have manufacturing facilities can activate their own developments
We, Intro Bio Pharma Inc., will keep fulfilling our duty to develop the domestic pharmaceutical industry, contributing to promotion of the national health, and create the better future.