The Impact Of ePRO On The Patient & Site Journeys
Source: Castor
Explore the transformative impact of electronic Patient Reported Outcomes (ePRO) from two crucial perspectives: the patient and the clinical site. Join our solutions experts as they demonstrate how Castor ePRO can enhance your clinical trial by improving the patient experience and streamlining site operations.
Agenda Highlights:
Empowering the Patient Journey
- Patient-Centric Approach: Discover how ePRO places patients at the center of clinical trials, enhancing their experience and engagement.
- Reducing Patient Burden: Learn how ePRO can minimize unnecessary and lengthy site visits, making participation easier and more convenient.
- Inclusive Trials: Understand how ePRO contributes to more inclusive trials with better data quality, applicable across various study types.
Optimizing the Site Journey
- Efficiency in Data Collection: See how ePRO reduces the administrative burden on sites, enabling more efficient data collection and management.
- Automation and Compliance: Learn about automating patient surveys, reducing manual tasks for site staff, and tracking survey compliance rates effortlessly.
- Reliable Data: Explore how ePRO provides clean, reliable data that complies with ALCOA+ standards, ensuring high-quality outcomes.
See It in Action
- Live Demos and Use Cases: Get a practical look at how Castor’s technology supports both patient and site journeys through real-world examples and live demonstrations.
Watch now to understand how Castor ePRO can revolutionize your clinical trials, making them more patient-friendly and efficient.
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