Unlocking Innovation: Embracing Validation 4.0 for a Digital Pharma Future
Complimentary
Learning Level: Intermediate
Time: 1000 - 1100 ET
Session Length: 1 hour
The pharmaceutical industry faces increasing pressure to accelerate drug development while controlling costs, enhancing quality, and ensuring safety. Traditional validation practices often act as a bottleneck, hindering innovation and preventing the full adoption of digital advancements. This webinar, based on the ISPE Good Practice Guide: Validation 4.0, will introduce attendees to modern validation thinking in an increasingly digital world. We will explore how Validation 4.0 builds upon foundational principles of Quality by Design, Quality Risk Management, and Knowledge Management, leveraging today’s modern technologies
Despite two decades of regulatory recommendations for flexible approaches, many companies remain entrenched in conventional methodologies. This session will highlight the paradigm shift Validation 4.0 represents, moving beyond fixed validation runs to a vision for more efficient, real-time evidence generation within a digital environment. Learn how this approach facilitates rapid evolution while maintaining verifiable control over products and processes, ultimately enabling faster time to market and a continual improvement culture. We will discuss the need for scalable solutions to manage increasing data volumes and ensure robust data quality and integrity for GxP purposes and emerging technologies like AI and Machine Learning. Don't let legacy validation practices impede your ability to innovate; discover how Validation 4.0 can transform your manufacturing operations.
Learning Objectives
- Understand how Validation 4.0 leverages foundational principles (QbD, QRM, Knowledge Management) to overcome traditional validation bottlenecks.
- Learn how Validation 4.0 represents a paradigm shift from fixed validation runs to more efficient, and can enable real-time evidence generation, enabling faster time to market and continual improvement.
- Discuss 1-2 case studies to demonstrate this approach in the real world.
