Accelerating Biopharmaceutical Development

Monday, February 25, 2013, 8:30am-9:45am PST

This session will focus on how best to leverage prior process, analytical and formulation knowledge toward acceleration of drug substance and drug product manufacture. The value of clear understanding of the link between process parameters and CQAs will also be explored. Some examples could be minimal or no process development for phase I material, more efficient process and product development and more streamlined process validation.

Confirmed Speakers

Ann Lee, Genentech

Joe Miletich, Amgen