TAPROOT

FOR PATIENTS

Taproot Health - For Patients

TAPROOT

FOR PATIENTS

Taproot Health - For Patients

TAPROOT

FOR PHYSICIANS

Taproot Health - For Physicians

TAPROOT

FOR PHYSICIANS

Taproot Health - For Physicians

EVERYDAY OVER 1600 PEOPLE DIE FROM CANCER IN THE UNITED STATES
  • RESPECTING THE PATIENT
  • REALIZING HIGH-QUALITY DATA
  • REWARDING OUR PARTNERS

Developing personalized treatments for cancer patients requires a great deal of quality information that currently either does not exist or exists mainly in individual physician clinics, making it inaccessible.

Data That Matters. Outcomes That Make a Difference.

DATA THAT TRANSFORMS

No more small and incomplete data sets
We collect regulatory-grade data from community and academic centers across the nation. Complete patient outcomes are linked to detailed biomarker data, providing a complete picture of care.

UNITY THAT HEALS

No more going it alone
Cancer is too big of a problem for any one group or company to solve. We need to come together to collect and share the data that is needed.

PERMISSION MATTERS

No more working around the patient
Patients consent to collect and share their data to advance research and cancer care.

REVENUE SHARING THAT HELPS

Providing value for data
Clinics are required to do more with less, especially when conducting research. Net revenue is shared with clinics to enable the necessary data collection. This revenue can also fuel further research and improve patient care.

THE NETWORK

Taproot empowers
clinics to collect and share data

We need a national, high-quality cancer database. Taproot Health, is making it a reality. Our network is built by oncologists for oncologists, and their patients. Community and academic centers are motivated to work together. Physician time is protected by using simplified data collection methods that seamlessly integrate with clinical workflows. Scientists have direct access to de-identified data for research. Clinics share in any net-revenue to advance personalized medicine.

THE PLATFORM

Regulatory grade data on every patient

Databases are only as good as the underlying data. ROOT has been designed as an end-to-end solution, focusing on quality and quantity of data through the following methods or standards:

Multi-stakeholder prospective clinical data protocol
AHRQ/Medicare compliant patient registry design
Standardized, consensus-driven data elements and data dictionary
Patient consent management
Clinic training and certification

Detailed files types
Blockchain like public ledger for transparency
HIPAA compliant security
Healthcare information technology standards (HITSP)
Data analytics and reporting