Preclinical and Clinical Bioanalytics

Bioanalysis Is Generally Used To Determine The Quantitative Measurements Of A Compound Or Its Metabolites In Blood, Plasma, Serum, Urine, Or Tissues

Bioanalysis provides critical information to support all phases of product development.

dicentra provides method development, validation, stability testing, and sample analysis for every phase of your clinical trial at our state-of-the-art research facility. Our team of experts specializes in developing and validating bioanalytical methods for PK/TK sample analysis using ultra-performance liquid chromatography-mass spectrometry (UPLC/MS/MS) as well as liquid and gas chromatography.

Our bioanalytical services are GLP and GCP compliant and follow Health Canada and US FDA guidelines. Our mission is to provide accurate and reliable data that is subject to rigorous scientific and regulatory review, ensuring the success of your discovery, preclinical and clinical programs.

Our bioanalytical services are available for:

  • Pharmacokinetic (PK)
  • Bioavailability Studies
  • Bioequivalence Studies
  • Drug Interaction Studies

Learn more about how our preclinical and clinical bioanalytical services can elevate your clinical trial.