Multiple-Attribute Monitoring at Peptide or Subunit Levels: Ready for QC!

Learn How to Effectively Implement MAM in a Regulated QC Environment

Multiple Attribute Monitoring (MAM) is a method used to concurrently analyze various critical quality attributes (CQAs) of biotherapeutics. It uses mass spectrometry techniques for comprehensive product characterization, batch variability tracking, and stability monitoring. Achieving consistent results using MAM usually requires highly standardized procedures, careful calibration of equipment, and rigorous data analysis protocols.

Key Learnings:

§  See study results of the effective implementation of MAM, ready for a regulated environment

§  Understand the applicability of MAM at the peptide level using a simple LC-MS platform and 21 CFR Part 11 compliant-ready software

§  Learn how automated data processing can maintain the integrity and quality of data and streamline the MAM workflow