Kronos Science has extensive experience in custom development of a wide variety of assays.  Assays not currently on the test menu can be developed and set up to meet specific client needs.

KS specializes in bioanalytical and pharmaceutical research studies, such as PK analysis, bioequivalency studies and pharmacokinetics for the pharmaceutical, biotechnology, clinical research industries and academic institutions.  KS is committed to performing to the highest standards as an extension of a client’s research and development programs.  As Kronos Science is CLIA certified and compliant with Good Laboratory Practices (GLP), the research and development will be done in full observance of all appropriate regulations and standards.

KS provides method development, modification, and validation of custom assays in a wide variety of biological matrices using LC/MS/MS, LC/MS, HPLC with UV/VIS & fluorescence detection, GC/MS, GC/FID, UV, ELISA, RIA and enzymatic methodologies.  KS method validation includes, but is not limited to, sensitivity, specificity, recovery, accuracy, precision (intra & inter), linearity, reference ranges, stability, bio-variation, and correlation studies.  All methods are validated to document the performance of the method in KS’s laboratory before conducting sample analyses.  KS supports preclinical trials and all phases of clinical trials.

For additional information or to discuss a desired assay, click here