In this webinar, we will present key insights from preliminary findings by the TUFTS Center for the Study of Drug Development, exploring how a comprehensive model that brings CDMO and CRO services under one roof can significantly impact the expected Net Present Value (eNPV) of drug development programs. We will demonstrate how streamlined services across drug substance, drug product, and clinical research can enhance efficiency, reduce timelines, and ultimately deliver high-quality therapies to patients faster. Key takeaways include:

Gain a comprehensive understanding of both the scientific and practical considerations in peptide drug development for oral administration. Join us for a deep dive into:

All new biologics begin at the bench with process development, but the ultimate goal is to bring the process to the production scale. Process development and bioprocess scale-up present many challenges, including maintaining consistent and reproducible growth kinetics, productivity, cell health, and mass transfer. This conversation will focus on strategies to meet these challenges for scaling from bench scale to pilot scale, including effective control strategies for process parameters such as agitation, dissolved 02 and CO2, and nutrient supplementation to ensure optimal cell performance and product yield. Join experts from Thermo Fisher Scientific as you will learn:

Thermo Fisher explores the role of qPCR and dPCR tools in fast-tracking biologics development. Find out more about:

Examine the key indicators of CDMO quality performance, as identified by high-performing biotech organizations. Gain new insights into how a holistic application of quality impacts all measures of product success. Download now to understand:

Learn why quality is so important, not just in drug development and manufacturing, but also in your CDMO partnerships, where identifying criteria for quality is critical to fostering excellence in every interaction and process. Download your free blog now for a look at:

Explore the risks of poor solubility and bioavailability and discover how the use of predictive modeling in pharmaceutical research is playing a critical role in helping to overcome these issues. Download now for an informative look at:

Discover how Thermo Fisher Scientific’s expertise, capabilities, and capacity were key factors in facilitating flexible solutions to meet an enormous, global demand. Your free case study explores:

Read your free blog for new insights into quality harmonization’s role in enhancing the resilience and efficiency of the supply chain by fostering consistency, reliability, predictability, and operational agility. Capture an inside look at: