In our newest blog post, we partnered with Sitero to dive into a comprehensive case study of a phase 3 trial involving 140 research sites across Australia, Canada, and the United States, comparing the performance of sites using CRIO’s eSource platform with those that aren't. From improved enrollment efficiency to a reduction in protocol deviations, CRIO’s technology is transforming the way clinical trials are conducted, leading to more reliable and timely results. If you’re involved in clinical research and looking to optimize your trials, this blog post is a must-read. ??: https://bit.ly/4gq6GCT
关于我们
CRIO is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system that enables a single point of data capture. As the leader in eSource technology, CRIO enables remote monitoring and immediate data review with a powerfully integrated eSource/EDC solution. The system delivers a single point of data capture, eliminating the need to re-enter data into EDC. At CRIO, our mission is to design and deliver a modern, intuitive and integrated software platform that reimagines clinical trials for quality, speed, and patient-centricity. CRIO keeps your source data secure and protects data integrity with built-in compliance across 21 CFR 11, ICH-GCP, GDPR, HIPAA, and other global regulations. Now you can bring trials to patients where they're at and access that data anytime, anywhere. For sites, CRIO is an enterprise tool for clinical trial management. For sponsors and CROs, CRIO serves as a single data platform for centralized monitoring. Our software frees you from inefficient, error-prone binders to capture source data. CRIO’s autofill and data validation tools reduce protocol deviations and save time. With patient scheduling, recruiting, financial management, and so much more, CRIO is an all-in-one enterprise solution for sites, sponsors and CROs.
- 网站
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https://www.clinicalresearch.io
CRIO的外部链接
- 所属行业
- 软件开发
- 规模
- 51-200 人
- 总部
- Boston，Massachusetts
- 类型
- 私人持股
- 创立
- 2015
- 领域
- Clinical Trial Research Studies、Data Management、Electronic Data Capture (EDC)、eSource、CTMS、Clinical Trial Management System、Medical Research Studies、clinical data management、eClinical Solutions、Clinical Research Organization (CRO)、Clinical Research Sites和Patient Stipends
地点
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主要
获取路线
US，Massachusetts，Boston，02111
CRIO员工
动态
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?? Revolutionizing clinical trials with eSource! Our latest case study explores how eSource can dramatically improve trial efficiency and reduce costs across the clinical research ecosystem. Here's a quick highlight: "Direct data capture can streamline processes, leading to potential savings of 30%+ on monitoring and data management costs." What's one way you see sites, sponsors, or CROs benefiting from eSource adoption? ?? Comment below with your thoughts! Curious about the full picture? Let's connect to discuss how these insights could transform your trial operations! ??: https://bit.ly/4csdvkx #eSource #ClinicalTrialInnovation #ResearchEfficiency
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CRIO Welcomes Inato to the Partners Program! Inato’s free clinical trial marketplace helps sites:? -View open and upcoming trials -Get personalized trial recommendations -Showcase your site’s unique strengths to stand out to sponsors NEW: The NEW Business Development category in the Partner Directory makes it easy for CRIO sites to quickly find and start using Inato’s marketplace, helping CRIO sites get matched with the right trials faster. Explore their listing for quick and easy sign-up! Find instructions in our blog post.? ?? https://lnkd.in/eNjDhKaM Attending the Upcoming Society for Clinical Research Sites (SCRS) Global Conference? Visit Inato at booth #123 and CRIO at booth #401 to learn how this partnership can help you connect with the right trials and sponsors!
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CRIO Welcomes Patient Qualifier as a Certified Integration Partner! Patient Qualifier's recruitment and lead management platform integrates with CRIO to optimize recruitment outcomes, helping CRIO powered sites operate more efficiently and effectively. Patient Qualifier offers the following Site Services: - Recruitment CRM - Campaign Development & Management? - Software Development CRIO users can explore Patient Qualifiers listing in CRIO’s Partner Directory, today! Instructions can be found in this Blog Post: ?? https://lnkd.in/edudk7WJ
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Our latest blog post is live, and it’s packed with insights on how Trially’s cutting-edge technology enhances EMR management and speeds up patient identification for CRIO sites. Key Takeaways: ● Streamline your EMR processes ● Boost recruitment efficiency ● Improve operational workflows Don’t miss out on discovering how CRIO sites can leverage Trially’s integration to transform their operational workflows and trial outcomes. Read the full blog post here: https://bit.ly/3AMimzD
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How do you think real-time data capture could impact your clinical trials? Share your thoughts below! Curious about the numbers? Here's a teaser: - 30%+ potential savings on monitoring and data management - Increased efficiency for sponsors, CROs, and sites Want to dive deeper? Here’s a link to our recent case study: https://bit.ly/4csdvkx #ClinicalResearch #Innovation #DataManagement
How Sponsors Can Leverage New Technologies To Lower Trial Costs
clinicalresearch.io
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We are looking forward to joining DiversiTrials for this discussion on Friday! Check out Marc's post below for details ??????
Join the DiversiTrials team and discuss final impressions of the #FDA Guidance on #DiversityActionPlans and next steps. When: Friday 30-Aug-2024, 11:30am ET Where: https://lnkd.in/dD2a8eey Don't miss expert opinions from Daniel Fox, MPH, PhD, Mitchell Hilbe, Hadi Danawi, PhD, MPH ?. ???? ?????, Hannah Kulkarni of CRIO and yours truly. #Diversity #DEI #DAP #ClinicalResearch
DiversiTrials and Tribulations: FDA Guidance Community Forum FINAL
https://www.youtube.com/
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Join Marc Wartenberger and Hannah Kulkarni tomorrow at 11:30am EDT as they participate in DiversiTrials Podcast discussing the FDA Guidance Community Form Summary! ??: https://lnkd.in/dtnsy6UB
DiversiTrials and Tribulations: FDA Guidance Community Form Summary
https://www.youtube.com/
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New Blog Alert: Transform Your Patient Recruitment with CRIO and C6 | Site Solutions! In our latest blog post, we dive into how the new CRIO-C6 partnership, powered by the CRIO Partners Program, is making patient acquisition easier than ever for clinical research sites. Discover the 3 key elements of a successful patient acquisition strategy and learn how our seamless API integration with C6 can help your site streamline recruitment, reduce costs, and lighten the load on your staff. Catch up on the full blog post here and see how you can leverage this powerful partnership to boost your recruitment success! ??: https://bit.ly/3T0sDOT #ClinicalResearch #PatientRecruitment #CRIOPartnersProgram
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