Key Elements Of Process And Analytical Development To Support Biologics Tech Transfer

Tech Transfer for biologic medicinal products is complex - filled with potential pitfalls, hazards, and breakpoints. Precision manufacturing must be coupled with speed to optimize processes and minimize risk. This webinar offers a comprehensive overview of key strategies and methodologies crucial for seamless technology transfer to Contract Development and Manufacturing Organizations (CDMOs).

Our expert panel delves into the complexities of technology transfer through the lens of real-world case studies. We investigate critical components for success, risk assessment, and effective mitigation strategies. Learn how to optimize your timeline and enhance efficiency in your transfer processes.

Our panel focuses on elements of process development that are relevant to the clinical and commercial scale manufacturing process – simplifying the scale-up process while reducing the risks associated with large-scale manufacturing.

• Examine both process development strategies for acceleration and scenarios where processes are developed from scratch.
• Discover how cutting-edge technologies alongside work sequence planning and parallel development strategies can expedite process acceleration.
• Gain insights into crafting tailored analytical panels that align with your specific process and product needs.

Lastly, explore the burgeoning outsourcing landscape in Poland and gain an overview of its economic landscape, infrastructure development, and the thriving life science sector. Discover the strategic advantages of leveraging Poland's academic centers, logistics infrastructure, and skilled biopharmaceutical human resources.