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Reducing the Burden of Data Collection in Oncology Trials

Jackie Brusch

Understanding patient reported outcomes (PROs) in oncology clinical trials enables researchers to develop more effective treatments for patients battling this illness. But if it isn't easy for patients to report their health data, they won't - so it must be accessible for them.

Electronic Clinical Outcome Assessment (eCOA) solutions allow seriously ill cancer patients to participate in clinical trials by offering them the ability to submit their data remotely, from the comfort of home, or at the hospital while receiving care. Patient-friendly features reduce burden, increase engagement and compliance, and ensure ALCOA principles are met for accurate, timely data capture.

Download the whitepaper to learn more about how eCOA is changing the way cancer patients contribute to finding a cure. 

About the Author

Jackie Brusch

Jackie Brusch is the Content Marketing Manager at CRF Health.

Previous Guide
Managing eCOA Data - Principles and Best Practices
Managing eCOA Data - Principles and Best Practices

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State of eConsent 2017 Report
State of eConsent 2017 Report