Biotechnologies Upstream & Downstream: Improve efficiency of your manufacturing process and quality of your finished product with QbD, PAT, Modeling, DOE, Capability tools

45-minute webinar aimed at illustrating the ease of implementation of QbD, PAT and Capability using a case study focused on biomedicine development.

Following the presentation, a 15-minute for questions & answers.

The objectives of QbD and PAT: Acquire an in-depth understanding and master the manufacturing process to ensure control of the final product, both in the development phase and in production.

This integrated approach to QbD, PAT and Capability, implemented with pragmatism and nourished by a wealth of experience and specific tools, will allow you to define development objectives:

• Identify critical sources of variability and associated risks.
• Guide product development.
• Install PATs and monitor Critical Quality Attributes (CQA) in real time, without requiring destructive methods and on a more representative sample.
• Deepen the understanding of critical sources of variability and their impact on the final product, thus promoting their control.
• Upstream
• Dowstream
• Filling and freeze drying
• Facilitate validation of the manufacturing process.
• Guarantee the state of control throughout production.

We invite you to participate in this webinar to discover how these concepts and methodologies can be easily applied through a concrete case study in the field of biotech Pharma manufacturing.

Register now!