Mastering QbD For Successful Process Validation Campaigns And Commercial Manufacturing Of Biologics

Quality by Design (QbD) has revolutionized the landscape of biologics manufacturing and quality assurance by moving away from the traditional focus on end-product testing and instead emphasizing a deeper understanding of the manufacturing process and the importance of design control. This paradigm shift allows biopharmaceutical companies to proactively identify and address potential risks, ultimately accelerating development timelines, reducing production costs, and ensuring that biologic products meet the highest standards of safety, efficacy, and overall quality. By integrating QbD principles into every stage of development, companies can optimize their processes and minimize costly setbacks.

In this webinar, industry-leading bioprocess experts will explore the challenges and opportunities that arise when implementing QbD in biologics development and manufacturing. Through an in-depth case study, participants will gain valuable insights into how QbD principles can be applied in real-world drug product development, overcoming obstacles, achieving optimal outcomes, and streamlining the process to deliver life-saving biologics to patients more efficiently. This session will provide key takeaways for anyone looking to enhance their QbD strategy and ultimately improve the speed and quality of biologic product development.