Webinar: Biopharma CE Method Compliance in a Global Market
Learn about the current biopharmaceutical industry standards for method validation, transfer and control (i.e., system suitability) using capillary electrophoresis (CE) methods as examples. This webinar will highlight global regulatory expectations for method compliance that may not be directly stated in ICH Q2R1.
Key Learning Objectives
Updates on current industry standards for method validation, transfer and control
Method compliance that may not be addressed in ICH Q2R1
What you must know now for the May release of USP 129 Who Should Attend Biopharma Analytical Development and QA/QC Researchers, Lab Managers, and Directors.
Presenter: Dr. Chantal Felten Owner, Alpine Analytical Academy Speaker Bio