While biotherapeutics is one of the fastest growing sectors in life sciences today, the tech transfer process still takes many years. Regulatory approval can be time consuming—from conducting clinical trials to achieving a validated process design.

In this on-demand webinar, Dr. Monica Lomeli, Pharma Principal Solution Consultant at AspenTech, and Dr. Mark-John Bruwer, Senior Director of Strategic Product Marketing at AspenTech, discuss how regulators, such as the FDA, are implementing process modeling and simulation to accelerate knowledge creation for faster, more efficient system design. Learn how innovations including mechanistic and hybrid modeling enable you to:

• Rapidly design for optimal yield, shorter cycle time and robust operation
• Gain new insights into the optimization of downstream purification processes
• Leverage the same science- and engineering-based approach used by regulators

Watch to learn how you can expand your toolset to advance tech transfer and accelerate regulatory submissions.