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Strategies for robust process characterization and validation to accelerate biologics manufacturing
Webinar on demand
Establishing strong process characterization and validation early is critical to ensuring biologics are developed efficiently, in compliance, and ready for scale—but these steps are often underestimated and overlooked until late in development.
In this webinar, experts from Thermo Fisher Scientific will share real-world examples that uncover commonly overlooked steps and how to create a robust, data-driven process design to help accelerate validation readiness and reduce manufacturing risk.
Together, we will learn how partnering with a CDMO early and an integrated approach to process understanding can help you move faster from development to commercial success.
Key takeaways include:
- A toolbox of strategies for an efficient technology transfer
- Design and execution of robust process characterization and validation
- Data-driven validation approaches for early-phase development and commercial manufacturing
Helpful resources
Webinar
Preparing your biologic for commercialization: strategies to reduce risk and optimize outcomes
Leverage the experience of a top CDMO for best practices including how to remain flexible in the face of uncertain market demand, identifying the best practices to a reliable execution, and optimizing the latest digital tools to reduce risk to your timelines