Breakout I
Beyond Sponsor Mandates: Leveraging Technology As A Site Asset
With sponsor-required tools and platforms piling up, sites must find ways to make technology a long-term asset rather than a short-term burden. This session covers strategies for integrating technology smoothly into site workflows, enhancing efficiency, and supporting patient care. Experts will share best practices to help sites adopt and scale tech solutions that add ongoing value to their operations.
Decoding FDA Guidance: Digital Health Technologies & GCP Oversight
Join this essential session as a panel of experts unpack the latest FDA guidance on digital health technologies (DHTs) and technology use in clinical trials. Gain clarity on what Good Clinical Practice (GCP) and other regulations truly require in terms of oversight and technology implementation. With ambiguity still surrounding these topics, this session will demystify key aspects, address common misconceptions, and provide actionable insights for research sites and sponsors.
Enhancing Patient Experiences With Tech-Driven Care
Discover how clinical trial technology can enhance the patient experience by addressing disparities, fostering trust, and streamlining interactions. This session will explore practical strategies and best practices for integrating technology to overcome bias, promote fairness, and deliver patient-centered care. Join the discussion to learn how empathy and innovation can drive impactful outcomes in clinical research.
Understanding Cybersecurity & Licensing Challenges
As clinical research increasingly embraces digital solutions, cybersecurity risks and complex licensing hurdles are top of mind. This session will explore key strategies for protecting sensitive data, addressing emerging threats, and navigating the evolving landscape of licensing requirements. Leave with actionable insights to enhance data protection, ensure compliance, and fortify your operations.