This session will explore a forward-looking vision for Pharma and Biotech manufacturing that transcends traditional Manufacturing Execution Systems (MES). As MES evolves, manufacturers are adopting adaptable, modular solutions that ensure interoperability, flexibility, and easy configuration. By prioritizing people and processes, companies can optimize manufacturing efficiency while enhancing data integrity and compliance, leading to significant operational improvements. In this session you will learn more about how to:

Manage the production process and quality in real time from order to batch release in one browser-based user interface visualizing real-time and historical data.

• Digitize all direct batch execution (EBR) and execution related activities (Logbooks and Digital Procedures) to eliminate paper or unstructured electronic records where data is trapped.
• Leverage out of the box and configurable functionality on a no-code platform.
• Analyze and report on operational data in one place for a single source of the truth.
• Achieve measurable results in cost reduction, risk mitigation, and revenue opportunities.