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The growing interest in personalized biotherapeutics has resulted in the development of diverse molecule pipelines and improved manufacturing approaches that save time, improve processes, and ensure a high-quality final product. However, manufacturing process challenges remain, and these must be addressed to produce and deliver enough of these complex therapies to patients.
In this GEN webinar, our experts will present robust solutions for meeting the demands of clinical and commercial manufacturing of biotherapeutics. They will introduce Cytiva’s Fast Trak bioprocessing solutions and describe how the Process Development and Validation Services team can work with scientists to speed up their drug development and get therapeutic molecules to the clinic faster.
A live Q&A session followed the presentation, offering a chance to pose questions to our expert panelists.
Director, Fast Trak Process
Development Services
Cytiva
Team Manager, Fast Trak Process Development and Validation Services
Cytiva
Webinar produced with support from:
