
ABOUT CRIO
CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines data collection and management, ensuring protocol compliance and reducing errors. By eliminating paper binders and automating workflows, we help clinical sites and sponsors save time and money, improve data quality, and enhance patient safety. Our digital-first, site-centric approach supports virtual, hybrid, and traditional study structures, making clinical trials more efficient and effective.
CASE STUDIES
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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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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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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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Explore the implementation of CRIO’s eSource solution by a leading pharmaceutical company to overcome process paralysis in clinical research.
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Explore the success story of an early-stage clinical pharmaceutical company that effectively navigated funding constraints when conducting its Phase 1 study without a third-party CRO.
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This study introduces sponsors to an innovative, lean, and efficient approach to data management that integrates site-facing technologies to streamline trial operations.
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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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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.
FEATURED SOLUTIONS
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Central eSource: How Sponsors Can Leverage Site Technology
In this presentation, CRIO founder and co-CEO Raymond Nomizu delves into how sponsors can leverage the electronic source trend among sites through the use of Central eSource.
CONTACT INFORMATION
CRIO
68 Harrison Avenue #605, PMB 32876
Boston, MA 02111
UNITED STATES
Phone: 617-302-9845
FEATURED ARTICLES
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Join industry experts as they discuss how the true value of DDC lies not just in the cost of the technology itself but in the operational efficiencies it unlocks.
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Join the Co-CEO of CRIO, as he explores research site challenges and how site-based technologies can reduce administrative burdens, enhance efficiency, and eliminate redundant one-time-use technologies.
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Lynn Bartholow is transforming clinical research for Native American populations. Explore her journey into clinical research and efforts to build trust and foster participation and community engagement.
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Learn how utilizing diverse data resources and collaborating with stakeholders enables sponsors to foster a culture of inclusivity, meet regulatory requirements and ultimately advance medical science.
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Remote Regulatory Assessments (RRAs) provide distinct advantages over traditional inspections, such as increased efficiency, reduced travel costs, and enhanced global oversight capabilities.
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Learn about the evolving U.S. clinical trial site market landscape including a detailed analysis of ownership models, market segmentation, and the role of financial investors in acquisitions.
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Examine the limitations of using Electronic Medical Records (EMRs) in clinical research compared to eSource systems.