We are compliant with U.S. FDA cGMP/GLP standards as well as ICH for all levels of clinical development. We employ these standards that are phase-appropriate for your clinical development or research.
GLP/GMP
FDA FEI: 30079962120
Cell-based Assays, Bioassays, Immunoassays, ELISA, MLR, PCR, qPCR, Flow Cytometry, RadioImmunoAssays, Transfection