CRIO to Collaborate with ArisGlobal
Cambridge, MA - Clinical Research IO (CRIO), a Cambridge-based technology company that has developed the first eSource system built and marketed directly to clinical research sites, announced today that it will collaborate with ArisGlobal to streamline clinical research.
CRIO’s system replaces the paper forms used at many research sites with an interactive web and tablet-based application. Using the system, researchers are able to configure eSource templates, and capture data quickly and accurately. By digitizing the collection of source data by investigators and integrating with other solutions, the company offers sponsors improved data quality and streamlined workflows.
Under the collaboration effort between CRIO and ArisGlobal, data captured electronically in CRIO will integrate with ArisGlobal’s agCapture, an electronic data capture system, and its integrated CTMS solution, thus eliminating double data entry and source data verification, two activities that consume up to 20% of the total time spent on a clinical trial.
“This collaboration is an excellent example of the cross-vendor collaboration required to resolve challenges in clinical research,” said Phuc Truong, co-founder of CRIO. “With this integration, we can give principal investigators and their staff an extremely user-friendly interface to collect data in way that’s consistent with their workflows, and ArisGlobal can deliver their life science sponsors immediate access to accurate data that does not need source verification.”
“Integration with Clinical Research IO further ours mission of offering life sciences companies a full lifecycle solution to enhance data quality and streamline operations,” said David Laky, Vice President of ArisGlobal – Clinical Solutions. “Many of our clients are looking for a solution to take out cost and time while enhancing data quality, and through this collaboration, we can deliver exactly that solution.”
Clinical Research IO (CRIO)
CRIO is the leading eSource solution for clinical research sites. Since its launch in September, 2016, it has signed up 50 research sites, and is now deployed on over 60 studies. For more information, visit www.clinicalresearch.io.
ArisGlobal
ArisGlobal’s cloud-based solutions facilitate global drug development and regulatory compliance within the life sciences and healthcare industries. Its cloud platform supports the entire product life cycle including clinical development, regulatory affairs, safety and pharmacovigilance and medical communications. Visit arisglobal.com, or follow ArisGlobal on LinkedIn and Twitter.
Empowering Sites and Patients: The Impact of Personalized Support in Clinical Trials
November 26th 2024To meet the growing demands of clinical research, sponsors must prioritize comprehensive support models, such as clinical site ambassadors and patient journey coordinators, who can address operational challenges and improve site relationships, patient satisfaction, and overall trial efficiency.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
FDA Finalizes Decentralized Clinical Trial Guidance
November 25th 2024The FDA's guidance is part of a broader effort to modernize clinical trials, improve efficiency, reduce participant burden, and expand access, particularly for underrepresented populations and those in geographically or economically constrained areas.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
