Right Data, Right Design: Making Clinical Trials Work for Patients and Sites

Session details:

This multistakeholder panel discusses how mindful, deliberate decisions about each data point can meaningfully reduce burden without compromising the ability to meet the objectives of a clinical study, and with the ultimate goal of bringing innovative medicines to patients as fast as possible. Key discussion points include how to:

• Make patient and site burden visible through real-life experience

• Confront disconnects between perceived value and lived impact

• Reframe “patient centricity” as a design responsibility, not a label

• Translate patient insights into actionable CDM influence
• Create a shared, human-centered commitment to change