This 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
Sean McCarthy Global Technical Marketing Manager Biologics SCIEX
Technology Networks Limited
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