Powders, Granules & Tablets: Improving Manufacturing Efficiency and Product Quality with QbD, PAT, Modeling, DOE, and Capability Tools

45-minute webinar to illustrate the ease of implementation of QbD, PAT, and Capability using a case study focused on the production of solid pharmaceutical forms.

Following the presentation, a 15-minute Q&A session will be held.

The objectives of QbD and PAT: Gain a deep understanding and master the manufacturing process to ensure the control of the final product, both in development and in production.

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

Define development objectives:

• Identify critical sources of variability and associated risks.
• Guided product development.
• Monitor Critical Quality Attributes (CQA) in real time, without 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.
• Raw materials & finished products: identification, impurities, sorting, etc.
• Mixing
• Processes (drying, granulation, compression, etc.)
• Facilitate the 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 solid pharmaceutical manufacturing.

Register now!