We envision an inclusive, intuitive, integrated system that generates, captures, and utilizes evidence to produce and provide the right treatment for the right patient.
Everyone should have the ability to participate--from health data donation to pragmatic trial participation.
It's basic science: clinical and non-clinical researchers must be able to learn from each other’s successes and failures.
Data and information are needed to inform decisions affecting health and healthcare.
Clinicians and payers need better information on what works for whom.