Developing Analytical Chromatographic Methods for Pharmaceutical Storage Stability Investigations
09 Dec 2016
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:
- Instrument and study considerations when developing stability indicating chromatographic methods
- Chromatographic method development factors, parameters and strategies
- A chromatographic method development case study using a Quality by Design (QbD) approach