Biosimilars: Lessons Learned
A Quality by Design approach to de-risk biosimilar development
Biosimilar drugs have become a mainstay of modern medicine with the latest reports stating the global market could reach $55 billion by 2020. The ever evolving landscape has led to different approaches to biosimilar development over the years.
Many sponsors now prefer a linear, orthogonal approach to biosimilar development starting at an early stage in an effort to de-risk the development pathway. In this webinar we will look back on the lessons learned from the past 10 years of biosimilar development and discuss how a Quality by Design (QbD) approach can help avoid costly mistakes, de-risk development and ultimately improve speed to market.
Join for this webinar on 29th June 2017 to develop a deeper understanding of how structure affects the functional activity of monoclonal antibodies and how this can be used to make data-driven decisions throughout development. Learn more about the evolving biosimilar development pathway and how a QbD approach ensures a step-wise, orthogonal process to de-risk development and improve speed to market.