Improve Bioprocess Freezing Outcomes With Analytics And Testing Services

Developers and manufacturers are facing a need for actionable data that allows them to make informed decisions about what changes need to be made to optimize results. While AI is exciting, there are many shorter-term and more tangible things that can be done in the biopharmaceutical sector; such as using fewer materials or achieving better utilization of the materials that you have, an analogous thing can be considered for knowledge workers that has led to a trend of outsourcing work to CDMO partners to get drugs to market faster. The other trend that is gaining popularity is making phase appropriate choices for verification and validation studies.

This webinar demonstrates multiple experimental case studies to showcase areas where developers can engage with Entegris to leverage subject matter expertise in experimental design, hardware, consumables, and contract services.

Key learnings

• Examining impacts of different treatments on homogeneity and particulate generation (including agitation, controlled rate freezing/thawing vs static freezing/thawing)
• Establishing comparability of first point to freeze last point to freeze in different types of equipment and different primary contact containers
• Discover options and benefits for surrogate material validation and verification testing
• See possible improvements by engaging process and material experts in real-world case studies