The Future of Clinical Trials: Integrating Technology and patient Experience
In this engaging interview, Edward Bartles, Associate Director of Solution Engineering at IQVIA, discusses the impact of digital health technologies and wearables on the clinical trials landscape. The conversation covers IQVIA’s strategic approach to embedding digital tools in the research process—from electronic clinical outcome assessments (eCOA) and IoT platforms to global device sourcing and real-time data collection. Edward explains how adopting e-consenting, connected devices, and flexible trial design reduces patient burden and improves engagement across multi-region Phase III studies.
Special emphasis is given to regulatory trends, including decentralized trial implementation, EU clinical trials regulation, and the increasing flexibility behind trial methodology. The discussion highlights the importance of ensuring data quality, adaptability, and enhancing both the patient experience and clinical outcomes through innovative technology. Real-world examples showcase how integrating wearables efficiently sources data, improves patient support, and meets regulatory requirements, ultimately advancing pharma research.
Watch as industry expert Edward Bartles explores how clinical trials are rapidly evolving. Learn how digital health integration, wearable tech, and patient-centric innovation are shaping the future of clinical research. Discover practical insights into regulatory adaptation, improving patient engagement, and leveraging smart devices for superior trial outcomes.
