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Pharma MES 2023

Fueling the future of Life Sciences: unlock the next level of manufacturing excellence
September 24-26
Berlin, Germany

Capgemini is excited to participate in the next edition of Pharma MES, which will take place 24-26 September in Berlin.

Connect with Life Science industry leaders from around the globe and learn about the latest technological innovations in pharma and biotech manufacturing & operations.

The Life Science industry is facing a lot of pressure to achieve sustainable competitive advantages at a rapid pace and with a lasting impact. To compete in today’s market, Life Sciences organizations must embrace Intelligent and Sustainable Manufacturing principles to enable efficient, agile, and reliable end-to-end production, release, and delivery of therapies, as well as ensure that current good manufacturing practices (cGMP) are maintained and enhanced.

At Capgemini, we enable you to accelerate time to market at scale and to move together to the next level of performance by fostering the synergies between the Digital and the Engineering world. We help you to accelerate, scale, and secure your manufacturing transformation by leveraging our multidisciplinary digital expertise (in IoT, AR/VR, AI, IT, OT, and more) combined with deep domain knowledge. We build interoperable, connected systems obtaining a breakthrough in operational performance at scale. We are your global technology and transformation partner, from assessment to solution building, implementation, and validation, including harmonization, with operations in over 40 countries.

With us, unlock the next level of manufacturing excellence and get the future you want.

Our presence

Discover the latest technology innovations developed by Capgemini and meet with our top industry experts. 

Capgemini will be hosting 5 session rounds on “How to achieve a successful global MES/eBR deployment?” during this day at the World Café

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 sites implementations?
  • How MES/eBR deployment contributes to your sustainability targets?

Schedule a meeting with our experts at Pharma MES

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Life Sciences

Life Sciences organizations face a common challenge: to accelerate time to care – exponentially and at scale.

Meet our People

Laurent Samot 

Vice President, Head of Smart Factory / Digital Manufacturing 
As global head of the COE Smart Factory, Laurent is working with our digital manufacturing practices to implement the fourth industrial revolution: Industry 4.0.

Frédéric Burger Ph.D.

CTO Life Sciences and Regulatory Affairs, Global Life Sciences Center of Excellence Leader, Capgemini Engineering
Leading the global life sciences portfolio and solutions in Pharma and Medical Devices “This is undoubtedly a new stage in the use of data in the life sciences industry. With the combination of Regulatory Sciences and a clear strategy on Digital implementation, the data is now at the core of any new journey. We support our clients with expertise, strong assets and methodologies for accelerating their transformation”.