Bioanalytical method development & validation | Labcorp Drug Development Catalog
Sponsors and investigators need to prepare for quantitative analysis of targeted analytes and metabolites as part of drug investigations. Bioanalytical method development is a key component of a diverse array of processes, including human clinical trials and research model studies.
After successful analytical method development, you'll need to receive formal validation from regulatory authorities to ensure that the method's accuracy, specificity, robustness, reproducibility and other properties are compliant with regulatory guidelines.
Our analytical method validation services can help ensure regulatory compliance and clear communication between sponsors, investigators and authorities. Learn more about our bioanalytical services.
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Immunosorbent: ELISA (in vitro)
Monoclonal, Bioanalysis -
Bioavailability, bioequivalence and biosimilars modeling
Metabolism, Bioanalysis, IChem -
Drug-Drug interaction (DDI) studies
Metabolism, Bioanalysis -
Enzyme inhibition for drug-drug interaction (DDI) investigations
Metabolism, Bioanalysis -
OECD 505: Residues in livestock
Bioanalysis, Toxicology, Animal, Metabolite Identification