BIOanalytical Department of BLIRT S.A. provides analytical and bioanalytical services during drug development process and routine quality controls of raw materials or final pharmaceutical products. BIOanalytical Department was founded in 2011, as integrated part of BLIRT S.A biotechnology company. BIOanalytical Department of BLIRT S.A. is GLP and GMP – certified supplier of analytical and bioanalytical services for R&D, medical and quality control departments of biotechnology, pharmaceutical and CRO companies. The fully – integrated quality system with Good Laboratory Practice (GLP) has been implemented in 2011 while Good Manufacturing Practice (GMP) was granted in 2015. GLP certification ensures quality, integrity and reliability of the data. It is the key quality factor for successful drug development, registration and commercialization.