Event
Course Description
This 60 minute complimentary webinar describes some of the latest USP standards published as chapters in the United States Pharmacopeia – National Formulary (USP–NF). It will provide best practices for complex methods (e.g., host cell protein assays), validated test protocols for common biopharmaceutical methods (e.g., total protein and residual DNA assays), and a collection of platform tests used for particular product classes (e.g., monoclonal antibodies).
By taking this course, you will:
- USP’s biologics standards that are under development
- Development of and use of USP documentary standards (including general chapters)
- Recent new chapters designed for characterization of biologics
Who Should Participate:
- Analytical scientists
- QA/QC analysts
- R&D scientists and managers
- Manufacturing scientists and managers
- Contract research organizations
- Contract manufacturing organizations