Multi-Attribute Methodology (MAM) for Biotherapeutics Using LC-MS
Global Technical Marketing Manager Biologics SCIEX
presentation highlights how to implement a complete and easy-to-use MAM
workflow for biotherapeutic PQA monitoring using accurate mass LC-MS.
We will demonstrate how this new streamlined MAM workflow can be used to
track known impurities and identify new impurities using a single
software processing system that is as powerful as it is intuitive.
Learn how to reduce your analytical testing burden by incorporating LC-MS into the development process.
Key learning objectives:
- How to set-up and monitor PQAs using accurate mass LC-MS
- How to automate complex calculations for PQA and impurity levels and define limits for pass/fail flags
- How to track known impurities
- How to automatically flag unspecified impurities detected in a product sample