Comprehensive and perpetual informed consent allows for unparalleled access to health information, including clinical data, molecular data, and tissue that fuel virtually any precision oncology research.
- Access to any data and specimen collected in the course of routine cancer care
- Longitudinal and complete patient health records
- Pre-diagnosis
- Treatment course
- Post-treatment
- Patient can be re-contacted for additional data or research opportunities, including clinical trial enrollment
Learn more at orientcc.org
