The Life Sciences industry operates in a highly regulated environment, where efficient manufacturing processes and accurate documentation are essential for ensuring product quality, regulatory compliance, and patient safety. Manufacturing Execution Systems (MES) and Electronic Batch Records (eBR) have emerged as indispensable tools to streamline operations and enable Digital Transformation in this sector. However, deploying at scale a successful global MES/eBR solution requires careful planning, coordination, and adherence to regulatory requirements. Based on our experience, this session will provide you with valuable insights and practical strategies to achieve a successful global MES/eBR deployment. By examining real-world case studies and sharing best practices, Capgemini industry experts will empower attendees to navigate the challenges and complexities associated with implementing MES/eBR solutions across multiple sites and geographies, unlocking the next level of manufacturing excellence.
Our session will address the following questions:
- How to choose the right MES /eBR Solution?
- How to avoid digitalizing waste? The need for simplification, harmonization & standardization.
- How to accelerate and secure a global MES/eBR implementation (centralized or decentralized core model deployment, factory, library, automation, …)?
- Human at the core of global MES/eBR site implementations?
- How MES/eBR deployment contributes to your sustainability targets?
- How to measure the success of your MES implementation?
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