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Bioanalytical method validation is essential both for the qualitative and quantitative determination of the pharmaceutical drugs and their subsequent metabolites in different biological fluids. It plays a critical role in the evaluation of various aspects of pharmaceutical analysis – bioequivalence, bioavailability, toxicokinetic analysis, and pharmacokinetic analysis. Calibration Curve –  The calibration...
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Exploratory IND enabling studies are those wherein you have a limited exposure of the pharmaceutical drug products to humans. This IND application or the Investigational New Drug (IND) application is a pre-requisite of the USFDA regulatory norms before the start of actual toxicology studies in drug development. IND enabling...
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