Agile Quality by Design: A Practical Guide for Modern Pharmaceutical Development
Published on: Jan. 21st, 2026
Quality by Design (QbD) has become a cornerstone of modern pharmaceutical development, enabling teams to design robust products and processes through a structured, science and risk based approach. This webinar provides a practical and accessible overview of key QbD concepts, tools, and regulatory expectations applicable to all types of medicinal products.
Through a real-world case example, we will illustrate how the agile QbD method can be applied from early development and how they support regulatory interactions and successful submissions. The session will equip participants with a clear understanding of how to integrate QbD into their development strategy and how to leverage it to enhance product quality, efficiency, and compliance.
This webinar is based on material developed by Cybernano and VCLS for an eLearning programme commissioned by EIT Health and the European Commission. Drawing on this work, we will explore the core principles, tools, and regulatory expectations of Quality by Design (QbD) applicable across pharmaceutical development.
Agile Quality by Design: A Practical Guide for Modern Pharmaceutical Development
Through a real-world case example, we will illustrate how the agile QbD method can be applied from early development and how they support regulatory interactions and successful submissions. The session will equip participants with a clear understanding of how to integrate QbD into their development strategy and how to leverage it to enhance product quality, efficiency, and compliance.
This webinar is based on material developed by Cybernano and VCLS for an eLearning programme commissioned by EIT Health and the European Commission. Drawing on this work, we will explore the core principles, tools, and regulatory expectations of Quality by Design (QbD) applicable across pharmaceutical development.
