Developing Analytical Chromatographic Methods for Pharmaceutical Storage Stability Investigations

Library Number:

WEBC134969485

Author(s):

Dr. Thomas Swann

Source:

SelectScience

Content Type:

On Demand Webinar

Content Subtype:

Compliance and Regulatory

Related Products:

Small Molecule Method Development

Abstract / Summary

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

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.