Webinar: Utilizing USP Standards and Tools to Support Development of Monoclonal Antibodies and Gene Therapy Products

In this webinar “Utilizing USP Standards and Tools to Support Development of Monoclonal Antibodies and Gene Therapy Products” Ms. Niomi Peckham (United States Pharmacopeia, or USP) discusses a series of platform reference standards developed to support the development and manufacturing of monoclonal antibodies (mAbs) and gene therapies (e.g., AAV). She demonstrates how to incorporate these standards into your development programs, including showing representative data and case studies. Dr. Chris Heger (Bio-Techne) describes how to use the mAb and AAV reference standards for charge and size variant analysis in icIEF and CE-SDS methods, respectively, using Maurice instruments.