Case Study
Monday, March 23
11:55 AM - 12:20 PM
Live in Everett
Less Details
Traditional MES deployments are often costly, time-consuming, and rigid—frequently tailored to a single product rather than the diverse needs of modern pharmaceutical manufacturing. In 2025, an agile electronic batch record (eBR) approach was introduced to address these challenges, aiming to shorten lead times, lower costs, and make MES adoption feasible for a broader range of manufacturing sites. By rethinking recipe configuration and applying flexible process parameterization, this next-generation MES concept enables adaptation across multiple products without extensive re-engineering. The session outlines the strategic drivers, design methodology, and implementation insights behind creating a more adaptable and scalable MES framework. In this session you will learn how to:
Experienced Information Technology Site Lead with a demonstrated history of working in the pharmaceuticals,Biologics and Cell Therapy manufacturing industry. Skilled in MES,Laboratory Information Management System (LIMS), SAP Implementation, Manufacturing Systems, Computer System Validation, and IT Business Strategy. Strong information technology professional with a Master's Degree focused in Business Administration and Management, General from Fudan University.