Session (CTI)

Real-world evidence (RWE) is revolutionizing healthcare, but harnessing the power of routine patient health records for regulatory-compliant RWE studies presents unique challenges. In this session, we will explore the inherent differences between clinical trial and real-world data collection methodologies, address selection bias and ensure the inclusion of the right patients for your RWE study and evaluate the similarity of real-world data to clinical trial data and the role of analytics in ensuring quality and reliability of study results. We will review best practices for these RWE challenges to ensure that your data meets regulatory requirements. Sponsored by Corporate Partner, Cardinal Health