Register for this webinar to see how a composable approach to MES gives pharma manufacturers the flexibility to adapt quickly, enforce SOPs, and maintain data integrity — all while empowering frontline teams to build workflows tailored to their operations.
We will talk about:
What’s Driving Change: FDA digital compliance guidance, rising demand for personalized therapies, and the need to scale rapidly in response to new indications
Core Traits of Composable MES: What makes a system truly composable — and where legacy platforms fall short
How to Build It Right: Streamline operations with guided workflows, automated audit trails, and just-in-time training
Proof in Practice: Real-world results from pharma manufacturers improving speed, quality, and adaptability with composable systems
Whether you're navigating regulatory complexity, preparing for rapid scale-up, or modernizing legacy systems, this session will help you reframe how MES can work for today’s pharma environment.
Register for the webinar today!
Featuring:
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Olivier Neron
Global Head of Life Sciences Practice, Tulip
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João Aido
Digital Transformation Engineer, Tulip