It’s been a great 3 days here at SOS Save Our Sites in Oklahoma City! See you all next time Harrison Galusha Stefanie Palmer Raymond Nomizu Megan Richards Brook White Priscilla Huerta
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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CRIO partners 1nHealth stopped by to see us this morning at SOS Save Our Sites. Are you here too? Make sure to stop by! Brook White Stefanie Palmer Katie Walsh Ashli Bishop
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With a standardized, pre-mapped eSource template, Central eSource ensures sponsors and CROs consistency across sites while still allowing local flexibility. The result? Faster start-up, improved data quality, and seamless EDC integration. Want to learn how Central eSource is transforming clinical trials? Watch our on-demand webinar here: https://hubs.la/Q03bMWnC0
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CRIO's own Brook White spoke with Darshan Kulkarni this week about how to get the most out of attending conferences! Check out the full discussion below ??????
Conferences are more than just networking—they’re about building relationships that lead to real business growth. Brook White and Darshan Kulkarni explain how to turn every interaction into a lasting client opportunity. #SOS2025 #clinicaltrials #networking #kulkarnilawfirm #klf
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CRIO转发了
We're excited to be part of #SCDM 2025 EMEA in Brussels this April! ??? Check out this video from our Co-CEO, Jonathan Andrus, on what to expect! ??
The #SCDM 2025 EMEA Conference is almost here, and we’re excited to bring together the brightest minds in clinical data management and dive into some truly transformative discussions.?No matter where you are in your #CDM career journey, #EMEA25 offers something for everyone. Here's what Jonathan Andrus, our #SCDM Treasurer, has to say about what you can expect: ? World-class sessions on clinical data management, emerging #technologies, and industry best practices ? Actionable insights into #data standards, regulatory compliance, and the future of data #analytics ? Networking opportunities to connect with like-minded professionals and industry leaders ? Learn how to use data as a catalyst for curiosity and a guiding force for patient-centric #trials. Don’t miss out on the must-attend event for clinical data managers in Europe, register today and be part of the conversation on 9-11 April in Brussels: https://lnkd.in/e3tHzZRP Joanna Florek-Marwitz Richard Hogan Paulina Szczepaniak Ward Lemaire Carol Schaffer Patrick Nadolny Dawn Kaminski Dr. Deepak Kallubundi CCDM?, CPM Manny Vazquez, CCDM Maria Craze Ram Mudaliar Tanya du Plessis Magda Ja?kowska , Shobhit Shrotriya
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We're excited to be part of #SCDM 2025 EMEA in Brussels this April! ??? Check out this video from our Co-CEO, Jonathan Andrus, on what to expect! ??
The #SCDM 2025 EMEA Conference is almost here, and we’re excited to bring together the brightest minds in clinical data management and dive into some truly transformative discussions.?No matter where you are in your #CDM career journey, #EMEA25 offers something for everyone. Here's what Jonathan Andrus, our #SCDM Treasurer, has to say about what you can expect: ? World-class sessions on clinical data management, emerging #technologies, and industry best practices ? Actionable insights into #data standards, regulatory compliance, and the future of data #analytics ? Networking opportunities to connect with like-minded professionals and industry leaders ? Learn how to use data as a catalyst for curiosity and a guiding force for patient-centric #trials. Don’t miss out on the must-attend event for clinical data managers in Europe, register today and be part of the conversation on 9-11 April in Brussels: https://lnkd.in/e3tHzZRP Joanna Florek-Marwitz Richard Hogan Paulina Szczepaniak Ward Lemaire Carol Schaffer Patrick Nadolny Dawn Kaminski Dr. Deepak Kallubundi CCDM?, CPM Manny Vazquez, CCDM Maria Craze Ram Mudaliar Tanya du Plessis Magda Ja?kowska , Shobhit Shrotriya
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We’re excited to be attending Save Our Sites 2025 in Oklahoma City this week! If you'll be there, stop by Booth #3 to say hello or click here to book a meeting with us: https://hubs.la/Q03b9n4m0 #SOS2025 #SaveOurSites
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Don’t miss your chance to see how CRIO-powered sites are using Trially AI’s EMR-matching technology to streamline recruitment without adding extra work for site staff. What You’ll Learn: -How Trially’s AI-driven EMR integration helps identify qualified patients faster -Live demo of a seamless site workflow -Live Q&A to address your questions Register here: https://bit.ly/43qrQg6
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Protocol deviations are a common challenge in clinical trials, often leading to delays, added costs, and compliance risks. By transitioning from paper source to CRIO’s eSource, Benchmark Research cut protocol deviations by nearly 40%. This shift not only improved data quality but also streamlined workflows, enhanced patient safety, and simplified remote monitoring. Want to learn how they did it? Read the case study here: https://hubs.la/Q038CXf70
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If you'll be at the SCRS European Site Solutions Summit next week be sure to catch Marc Wartenberger's breakout session! Details are below ????
At CRIO, we support countless studies with decentralized elements. Join me and my fellow industry experts ? Clare Grace ?, Clare Campbell-Cooper, and Kalman Torocsik MD at the Society for Clinical Research Sites (SCRS) EU Site Solutions summit next week when we share key takeaways and insights. ??: Feb 25, 11am ??: Sala VII #clinicalresearch #scrs2025
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