Case Study
Tuesday, September 24
04:00 PM - 04:30 PM
Live in Berlin
Less Details
Explore the groundbreaking implementation of electronic Batch Records (eBR) across global manufacturing lines, revolutionizing efficiency and compliance. Delve into the nuances of biotechnology processing and the unique challenges it poses compared to traditional one-batch manufacturing methods. Uncover the pioneering efforts and innovative solutions required to seamlessly integrate eBR within the biotechnology sector. Discover the multi-active approach employed to address diverse regulatory landscapes and operational complexities, ensuring a comprehensive and future-proof solution. Join us as we navigate through the transformative journey of eBR adoption in biotechnology, driving industry standards to new heights. In this session, you will learn:
Brian DiVasta is Director for Computer System Validation for elevatebio for 3+ years. There his specialities are computer validation and quality assurance. Before his position at elevatebio he was with Sanofi for 8+ years as Associate Director, ITS Compliance.