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Nov 15, 2023 1:00 PM - Nov 16, 2023 6:40 PM

DIA Innovating Clinical Trials in Europe

This year's must-attend virtual live conference for pharmaceutical innovators and clinical researchers alike!


DIA Innovating Clinical Trials in Europe virtual conference will explore initiatives such as Accelerating Clinical Trials EU, European Health Data Space, and Digital Health Technologies. Dive into the groundbreaking potential of artificial intelligence (AI) in medicines development, reflect on the ethical considerations, ensuring fairness, privacy, and transparency, and gain insights into the regulatory perspectives and requirements. You will have the opportunity to learn how Real-World Evidence is transforming regulatory decision-making and putting patients at the center of discussions. Explore EU PEARL's master protocol studies in drug development and gain the knowledge and tools you need to stay ahead in this rapidly evolving field. Discover how Digital Health Technologies assist clinicians in facilitating identification, recruitment, and retention of patients, and explore the role of single-arm studies, standardization, and automation in innovative clinical trial design.


All of these are in the form of expert-led presentations, interactive panels, and thought-provoking sessions featuring the latest advancements in Clinical Trial Data. Register now for the DIA Innovating Clinical Trials in Europe!

Featured topics

    • Opportunities for Innovation in Europe
    • Integrated Research Platform concept
    • ACT EU
    • EU PEARL
    • European Health Data Space
    • Clinical Trial Data
    • Real-World Data
    • MetReal Cluster
    • Digital Health Technologies in patient recruitment
    • European AI Strategy
    • Novel Methodologies
    • Complex Clinical Trials


Want to learn more about DIA Innovating Clinical Trials in Europe? You've come to the right site!


Who should attend?

  • Participants Involved In:

    • Regulatory agencies (assessors, reviewers, inspectors)
    • Sponsors of non-commercial clinical trials
    • Biostatistics
    • Patient Organisations
    • Regulatory affairs personnel in clinical research
    • Professionals in charge of clinical trial strategy and conduction
    • Regulatory intelligence and policy professionals
    • Change managers for clinical trials business processes
    • Clinical research professionals working with submission, data, information sharing
    • Clinical safety professionals
    • Clinical operations
    • Data management

Program Committee

  • Álmath  Spooner, PhD
    Álmath Spooner, PhD Head of Europe Regulatory Policy & Intelligence (RPI)
    AbbVie, Ireland
  • Daniel  Millar, MBA
    Daniel Millar, MBA Senior Director, Strategic Business Transformation
    Johnson & Johnson, United States
  • Elke  Stahl, PhD
    Elke Stahl, PhD Senior Expert, Clinical Trials Department
    Federal Institute For Drugs and Medical Devices (BfArM), Germany
  • Jesper  Kjær, MS
    Jesper Kjær, MS Global Director for Public, Private Partnerships, Strat Ops, Global Med Affairs
    Novo Nordisk, Denmark
  • Fia  Westerholm, DVM, MSc
    Fia Westerholm, DVM, MSc Programme Assurance Manager
    European Medicines Agency, Netherlands
  • Estelle  Michael
    Estelle Michael RWE Policy & External Engagement Lead
    UCB, Belgium

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