Overview
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
Featured
Who should attend?
- Regulatory agencies (assessors, reviewers, inspectors)
- Sponsors of non-commercial clinical trials
- Biostatistics
- Patient Organisations
- The pharmaceutical industry and contract research organisations, including:
- 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 Máire Spooner, PhD, RPh • Chair
EFPIA IEGU working group, Belgium -
Daniel Millar, MBA • Senior Director, Strategic Business Transformation
Janssen Research & Development, United States -
Elke Stahl, PhD • Senior Expert, Clinical Trials Department
Federal Institute For Drugs and Medical Devices (BfArM), Germany -
Jesper Kjær, MS • Co-Chair, EMA/HMA Big Data Steering Group; Director of Data Analytics Centre
Danish Medicines Agency (DKMA), Denmark -
Fia Westerholm, DVM, MSc • Programme Assurance Manager
European Medicines Agency, Netherlands -
Estelle Michael • RWE Policy & External Engagement Lead
UCB, Belgium
