Presentation | June 2, 2020

In Vitro Test Methodologies For Characterizing Bioavailability Enhancing Formulations

Source: Lonza Pharma & Biotech

By Aaron Stewart, Associate Principal Scientist, Global R&D

Pharmaceutical Manufacturing

Improved methods are needed to evaluate the effectiveness of bioavailability-enhancement approaches.  This presentation covers the development of in vitro tools for characterizing bioavailability-enhancing formulations, criteria for selecting the optimal in vitro methods based on compound properties and dose, and case studies for multiple low solubility compounds.

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