Capturing the patient voice through eCOA—particularly ePROs—is key to understanding real-world treatment impact and side effect burden in cancer research. Medable’s oncology-ready eCOA platform enables this with built-in support for novel endpoints, long-term follow-up, and digital-first workflows that meet regulatory standards. In this session, learn how to streamline operations for sites with protocol-ready libraries and intuitive assessment design while remaining empathetic to patients and caregivers.Key learnings:

  • Learn how to strategically design protocols with digital endpoints, including long-term follow-up (LTFU), to meet regulatory expectations and support long-term data value.
  • Explore best practices for implementing eCOA solutions that reduce site burden and streamline workflows for clinical teams.
  • Gain insight into how digital-first approaches can improve patient engagement, site experience, and trial efficiency from startup through closeout.