We are providing the R&D service to establish the quality control document required for approbation of medication development and IND. Besides, we also can production and quality control document for clinical trials by using our GMP equipment. Therefore, we provide the best development and production support services for our clients.
Based on plentiful experiences and know-hows on technical transfer of the domestic pharmaceuticals’ medication technology, we are carrying out the research task to develop and transfer the generic medication technology that clients need. Especially, we are exceptionally experienced in production improvement through the dosage improvement research and successful development of generic medicine with the enhanced convenience to take.
Intro Bio Pharma Inc. has developed second-class and fourth-class medical apparatus and produced since GMP fitness authentication in 2017. Moreover, it is now proceeding with three-pole clinical trials in order to develop third-class medical apparatus, an conglutination inhibitor.