Course Description: 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.
Who Should Participate:
Scientists, managers, and regulatory experts responsible for the manufacture and testing of therapeutic proteins
The live version of this recording took place June 14, 2023
Access Duration:
Access to this course expires 60 days from the date of registration or until you mark the course ‘Complete’ – whichever occurs first.
Speakers:
Dr. Li Jing
Principal Scientist, Global Biologics
United States Pharmacopeia
Dr. Da Ren
FounderBioTherapeutics Solutions
Dr. Annu Uppal
Director, Scientific Affairs
United States Pharmacopeia