As the U.S. grapples with defining value in healthcare and medical interventions, there is growing recognition that integrating caregiver experiences and perspectives are vital to understanding a patient’s disease or condition journey. Yet, how to identify and collect relevant data from family caregivers to inform medical interventions remains in nascent stages.

Join us for a discussion on the value and importance of caregiver experiences, the current gaps in understanding of what matters most to caregivers, and how best practices for collecting this information to inform clinical, policy, and regulatory decision-making.