Electronic Patient Reported Outcome (ePRO)

Discover FDA’s guidance on collecting PROs for Real-World Evidence (RWE), focusing on timing, methods, and improving data quality.

The Evolving Landscape of eCOA in Clinical Trials Clinical trials have long grappled with the complexities of data…

Patient-reported outcome (PRO) instruments refer to multiple scales and questionnaires designed to collect patients’ personal feedback on their…

How Aktiia brought their continuous BP device to market by integrating vast amounts of blood pressure data with patient-reported outcomes

Electronic Patient Reported Outcomes (ePRO) can become a powerhouse for gathering high-quality data directly from patients. To help you navigate this journey, we’ve distilled five essential best practices for getting started with ePRO. These tips are designed to be straightforward and effective, ensuring you harness the full potential of ePRO technology.

Bring Your Own Device (BYOD) represents the future of eCOA, and prioritizes flexibility & convenience for trial participants. Read more now.

Shedding light on the complexities and advancements in measuring PROs, drug tolerability, and quality of life in cancer trials.

Learn how integrating Patient-Reported Outcomes (PROs) into clinical trials can drive success in Value-Based Care (VBC).

An avalanche of data from so many real-world sources is available today, with the promise of more data generated daily—so why not use it?

Castor’s ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own, might struggle with a technology solution that they’ve never used before.