Through real-world examples, including a live demo and case study where one sponsor saved over 200 hours per study launch by adopting a unified, standards-based approach, we’ll highlight how intelligent automation and AI can be practically applied to accelerate development.

Whether you are planning your first digitally enabled trial or optimizing an entire portfolio, this session will focus on lessons learned and frameworks that unify scientific consistency, operational deployment, and technology orchestration across oncology, metabolic disease, vaccines, and more.

Key takeaways include:

  • The value of standardizing digital instruments and processes across therapeutic area programs.
  • How intelligent automation and AI can drive repeatability, speed, and scientific rigor for sponsors.
  • Examples of tailored approaches in oncology, obesity, and vaccine studies.
  • Insights into the tools, teams, and practices that are shaping digital implementation in clinical research.