Patient Data Reporting Applications & Studies
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Biotech Delivers A Superior Patient And Site Experience
3/4/2025
To become the sponsor of choice for sites and patients in congenital hyperinsulinism clinical trials, a small biotech company prioritized delivering a superior experience while streamlining operations.
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Medable Beats Forecasted FPI Date While Raising eCOA Adherence In Japan
2/7/2025
A top-10 global pharmaceutical company aimed to address eCOA adherence and patient enrollment challenges faced by clinical trial sites and participants in Japan. See how they accomplished it and more with this case study.
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6 Key Ways Real-World Data Is Accelerating Breast Cancer Therapies
2/3/2025
Real-world data (RWD) is increasingly vital for advancing breast cancer research, and leveraging TA datasets allows researchers and clinicians to address pressing challenges.
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CRO Uses CRIO eSource To Double Monitoring Productivity
1/31/2025
Examine the transformative impact of eSource technology on monitoring productivity during a global Phase 3 trial conducted by a Contract Research Organization (CRO) amid the COVID-19 pandemic.
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Using Virtual Study Coordinators For EDC Entry And Query Resolution To Speed Up Data Access And Cleaning
1/31/2025
The piece showcases how the effective use of CRIO can significantly enhance site performance, supporting recruitment and diversity objectives for sponsors.
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CRIO And Sitero Partner To Drive Superior Enrollment, Speed, And Quality In Phase III Trial Using eSource
1/31/2025
Examine the partnership between CRIO and Sitero, including how it underscores the significant impact of technology in optimizing trial performance and accelerating treatment development.
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Breaking Free From Process Paralysis In Clinical Trials
1/13/2025
Explore the implementation of CRIO’s eSource solution by a leading pharmaceutical company to overcome process paralysis in clinical research.
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How Syneos Health Tackles Protocol Complexities
1/7/2025
Explore solutions employed by Syneos Health, a global contract research organization, to optimize Phase IIV clinical trials, particularly under a complex adaptive trial protocol.
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How eSource Reduced Benchmark's Protocol Deviations By Almost 40%
1/6/2025
Explore how a leading vaccine site network selected CRIO to help address the challenges with it's use of paper charts in collecting source data.
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Drive Superior Enrollment, Speed, And Quality Using eSource
1/3/2025
Explore a detailed analysis of 140 research sites involved in a Phase III trial, conducted by Sitero and utilizing CRIO’s eSource platform, which highlights significant advancements in trial performance and data quality.