Biomedical science is booming and troves of digital data are being generated daily. Yet, despite a digital transformation, the medical research enterprise cannot keep pace with the information needs of patients, clinicians, administrators, and policy makers. Outdated methods of enrollment, data collection, and follow up are slow, costly and have blocked necessary progress.
By empowering people with their health data, Hugo’s novel approach promotes partnership and enables access to comprehensive, longitudinal, real world data. This partnership presents the potential to build long term relationships with people that can extend across product life cycles.