HELP BUILD A NATIONAL ONCOLOGY DATABASE THAT BENEFITS EVERYONE.
A SHARED EFFORT
Working together as an oncology community
We can build something more powerful than anything we could build as individuals. Shared data increases research potential and value to advance care.
A PARTNERSHIP MODELClinics are treated as partners Partner clinics directly access data for research. They also share in any net revenue the data provides. There is transparency in data sharing and usage.
AN INNOVATIVE AND POWERFUL PROTOCOL AND DATABASE
Data must be complete and accurate Data must be collected in the right manner to be valuable. ROOT and its associated case report forms, data dictionary, molecular classification, data entry portal, training, and clinical flow provide regulatory-grade data.