An important aspect of pharmaceutical development is evaluation of a drug product's stability during storage. Such studies require a stability indicating method capable of measuring both the drug and the degradants that may arise during storage stability investigations. Achieving sufficient method selectivity, accuracy and precision for the various analytes potentially present can be challenging.
In this webinar, Dr Thomas Swann, Principal Scientist in the Technology Advancement group of Waters Corporation, will discuss:
Who should view this webinar?
This webinar is useful for analytical scientists interested in learning about developing chromatographic methods for the analysis of samples containing one or more main ingredients in the presence of degradants or other impurities.