
Digital Endpoint: Redefining Data Collection in Clinical Trials
Digital endpoints enable continuous, objective, and remote patient monitoring through sensors and wearables, improving data quality and the patient experience in clinical trials.
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Digital endpoints enable continuous, objective, and remote patient monitoring through sensors and wearables, improving data quality and the patient experience in clinical trials.
Download our expert guide to selecting the right ePRO tool for clinical trials. Enhance patient engagement, ensure data accuracy, and make informed decisions with our practical checklist.
Digital endpoints enable continuous, objective, and remote patient monitoring through sensors and wearables, improving data quality and the patient experience in clinical trials.
How Replior’s integrated UV monitoring improves patient engagement in the Almirall AKtive trial, a phase IV study.
The SCAPIS study collected and analyzed 30+ million data points from 30,154 participants with Replior.
Reflecting on 2023, this CEO message highlights Replior’s achievements, lessons learned, and steps taken to prepare for future growth and innovation in clinical trials.
SMS notifications in ePRO systems enhance clinical trial compliance by providing immediate, user-friendly reminders, leading to higher engagement and timely data submissions.
Download our eBook to solve retention, compliance, and data quality challenges in clinical trials with strategies from Replior experts.
Explore the roles of eCOA and ePRO in clinical trials, focusing on their impact on data collection, patient engagement, and patient-centric research.
Device provisioning ensures clinical trial participants have the devices they need, improving data collection, compliance, and inclusivity.