Process Analytical Technology (PAT) has become a cornerstone in modern pharmaceutical manufacturing, enabling real-time monitoring and control of critical quality attributes. This session will explore innovative PAT approaches, including plug-and-play measurement systems that integrate seamlessly within production processes. Attendees will gain insights into how PAT programs can be designed to improve process understanding, enhance product quality, and accelerate regulatory compliance, while maintaining operational efficiency across manufacturing sites. In this session you will learn how to:

• Design and implement a comprehensive PAT programme using innovative technologies for real-time process monitoring.
• Deploy plug-and-play measurement systems to track critical quality attributes seamlessly within manufacturing processes.
• Translate real-time process data into actionable insights that enhance process robustness, consistency, and regulatory compliance.

• Which critical quality attributes are most difficult to measure in real time, and what makes them challenging?
• How can plug-and-play measurement systems be integrated seamlessly into existing manufacturing processes?
• What strategies can turn real-time PAT data into actionable insights for improving yield and consistency?
• How can PAT programs balance innovation with regulatory expectations and validation requirements?
• What lessons from past implementations or other industries could inform a more successful PAT deployment?