Multi-Attribute Method (MAM) for analytical testing of biotherapeutics is gaining traction due to its potential to improve efficiency and provide more detailed information on product quality attributes (PQAs) as compared to conventional methods. This webinar will focus on the development of USP standards and tools to support MAM for product characterization and quality control. Considerations that impact the quality and consistency of MAM, approaches to enhance the method robustness, and case studies will be discussed.

Subject area:
Biologics

Objectives (If applicable):
N/A

Target Audience (If applicable):
Scientists, managers, and regulatory experts responsible for the manufacture and testing of therapeutic proteins