ePRO/eCOA White Papers & Case Studies
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Precise, Consistent, Faster Medical Coding For Clinical Trials
1/5/2026
Rave Coder provides medical coding for verbatim terms from Rave EDC and external sources using the MedDRA, WHODrug and JDrug dictionaries. Rave Coder centralizes and streamlines medical coding, delivering key benefits to sites, coding specialists and data managers.
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Clinical Data Studio: Unlock The True Power Of Clinical Trial Data
1/5/2026
Experience a transformative AI-powered data quality management solution that unifies study teams by providing seamless access to data from all clinical data sources.
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Expanding Clinical Research In East Africa With Digital Innovation
12/11/2025
Africa carries 25% of the world’s disease burden but hosts only 1% of clinical trials. Discover technology-driven strategies that close this gap and transform research access in underserved regions.
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Addressing Trial Design Hurdles Across Alzheimer's Disease Stages
12/10/2025
Explore how endpoint selection, rater training, and the strategic implementation of eCOA can help address the unique scientific, operational, and human considerations at each stage of AD.
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Study Analysis – Site Payment Automation
12/8/2025
By removing administrative bottlenecks, see how automation improves cash flow for sites, reduces operational burden for sponsors, and supports smoother, more predictable trial execution.
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The Real Cost In CNS Trials: Rater Drift And Site Readiness
11/21/2025
Learn how to build resilience into CNS trial operations with evidence-based frameworks that prioritize human factors alongside digital tools.
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Hospital-Based eCOA Implementation: Real Challenges In Infectious Disease Trials
11/21/2025
This resource outlines proven strategies to reduce delays, improve compliance, and meet regulatory standards for PRO data in infectious disease studies.
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Generate Regulatory-Grade, RWE With Speed And Efficiency
11/21/2025
For teams managing real-world evidence or post-market studies, automation offers a scalable solution to streamline workflows, maintain compliance, and accelerate decision-making.
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Simplifying The Patient Journey With One App
11/12/2025
A single mobile app simplifies clinical trial participation by unifying eConsent, IRT, and eCOA workflows, reducing patient burden and improving engagement across trial phases and locations.
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Improving Clinical Trial Performance Through Central eSource
10/23/2025
See how a top five pharmaceutical company leveraged our esource platform to enhance site performance, improve data consistency, and enable remote monitoring.