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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).

Should clinical trial companies collaborate to speed up innovation in AI, or is a healthy dose of competition needed for rapid advancements?

To gain a deeper understanding of eConsent, we have gathered the 10 most frequently asked questions that address the complexities of adoption, integration, and compliance measures

At DTxEast 2023, Castor joined a panel discussion to answer big questions when designing DTx clinical trials

eConsent plays a pivotal role in optimizing modern clinical trials, but the nuance around its adoption for pharmaceutical and medical device companies remains a consideration for implementation teams.