ePRO Resources
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Revolutionizing Pediatric Clinical Trials With ePRO And eConsent
10/16/2024
Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.
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Ensuring Patient-Centered Care In Oncology Trials
11/10/2023
In oncology trials, safety and tolerability are a core focus. From centralized ECGs to patient-reported outcomes, utilize this guide for optimizing assessments of drug safety and quality of life.
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ePROM Implementation: 4 Best Practices For System Functionality
2/13/2024
Explore four of the 15 system functionality considerations highlighted in an eCOA Consortium article that aim to create a more thorough and standardized approach to ePROM implementation.
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The Future Of Clinical Trials Rests On A Unified CTMS Platform
8/1/2022
Discover why a unified CTMS platform is the answer for managing both the clinical trial itself and the data it produces when it comes to poorly integrated clinical trial management systems (CTMS).
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Empowering Freenome: Large-Scale Data Quality And Compliance
10/17/2023
Delve into five ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.
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Leveraging Tech And Clinician Review To Improve Risk Detection
10/19/2023
Learn why neuroscience therapy developers should start adopting strategies to improve data quality and assess responses using a combination of technology and expert clinician review.
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Could ePRO Be The New Standard In Health Reimbursement?
1/30/2023
Recently, early-phase protocols have been collecting patient-reported outcomes (PROs) not only to get regulatory approval but to demonstrate value to public and private payers.
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Why Capturing Pro Data Matters In Early-Phase Oncology Trials
9/26/2024
If you are in the early stages of an oncology trial, there is a lot to consider when it comes to your data management and how the process can be simplified by improving how your study captures data.
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Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study
12/20/2024
This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.
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ISR Report Sheds Light On eCOA/ePRO Market Dynamics
5/15/2024
This comprehensive overview highlights the critical role these platforms play in modern clinical research, emphasizing their impact on data integrity and trial efficiency.