Castor Blog

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).

Are you facing data management challenges in 2024? Find us at ACDM, stand #7 and let’s discuss solutions to make your life easier.

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

Schedule a meeting with a member of the Castor team for a chat at SCOPE booth #222

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