Integrating Laboratory Information Management Systems with LC-MS/MS Systems for Incurred Sample Reanalysis

14 February 2011 by Thermo Scientific

Used for the quantitative determination of drugs and their metabolites in biological fluids, bioanalysis plays a significant role in the evaluation and interpretation of bioequivalence, pharmacokinetic (PK) and toxicokinetic studies. The quality of these studies, which is often used to support regulatory filings, is directly related to the quality of the underlying bioanalytical data. Bioanalytical methods used to support the drug development process are validated to ensure that they function in the manner in which they are intended. Methods must be robust and capable of producing accurate, precise and reproducible results that are appropriate for a specific analytical application and to satisfy FDA requirements.

Download this free whitepaper, by Joel Usansky of Thermo Fisher Scientific, to find out more.