Drug development requires preclinical studies prior to IND application which should be performed in GLP certified laboratories. There is no GLP certified preclinical testing facility in Turkey, which constitutes a significant barrier for new molecular entity development. IBG has established Drug Analysis and Control Laboratories which are in compliance with GLP regulations and Quality Management System.
Good Laboratory Practice (GLP) in an internationally recognized indicator of technical competence in pre-clinical studies. By providing official recognition of the competence of laboratories, it ensures a convenient method for identifying and selecting reliable test and analysis services for institutions in need of preclinical work for their molecules.
Güzide İdil TİLMENSAĞIR