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Event Details:
Some of the latest promising biopharmaceutical developments rely on antibody and antibody fragments that could be engineered for a variety of clinical applications. However, these next-generation antibodies, particularly antibody fragments, possess an increased level of complexity and technical challenges that may result in longer CMC development timelines and delays to clinical trials as well as commercial launch. In this webinar, experts will discuss formulation development and purification strategies to increase throughput, reduce operating costs and potentially decrease development times for monoclonal antibody fragments.