Reflections on the Summit The 2021 Global Site Solutions Summit, hosted by the Society for Clinical Research Sites, was an amazing event. The first in-person event that our company has attended in 18 months, the Summit provided an opportunity for CRIO to meet new people and reconnect with clients and friends alike. Post-Pandemic Trends, Here...
CRIO has been highlighted among the top solutions that help researchers track application deadlines, project milestones, and participant demographics. BOSTON, MA – August 24, 2021 – Clinical Research IO (CRIO), a Boston-based company working to transform the clinical research industry with the latest in the cloud and SaaS technology, has been named among the best...
In the latest virtual conference hosted by ACRP, Innovation in the Era of COVID, Raymond Nomizu of Clinical Research IO and Jessica Branning of ClinCloud Clinical Research discussed electronic Source (eSource) and how it has shaped the future of clinical research. Ms. Branning’s site, ClinCloud, was built ground-up on a technological platform centered around CRIO....
We recently passed Crohn’s and Ulcerative Colitis Awareness Week (December 1-7, 2020) and Clinical Research IO was interested in learning more about clinical research in gastroenterology. We connected with Gerry Glazer, Henika Lobo, and Dr. Michael Gould of TDDA Specialty Research (TDDA) to gain insight into conducting GI research. Can you tell us how TDDA...
Dr. James Clark of Charlottesville Medical Research recently had an FDA inspection of his site as it is a high enroller. He did not receive a FDA Form 483, and he was using the CRIO electronic source system on the study. Learn about his experience in this Q&A session. CRIO: What’s your background? Dr. Clark:...
Electronic Source (eSource) and Electronic Data Capture (EDC) are increasingly popular technologies for collecting and managing clinical trial data. The two types of systems are less similar than their names suggest. Interested in learning more about eSource? See why Clinical Research IO’s system is leading the industry by requesting a demo of our software.
Though Electronic Source (eSource) has been around for 10 years, it’s only recently started to gain momentum among clinical research sites. Why is now the perfect time for eSource adoption? This article, written by CRIO co-founder Raymond Nomizu, explains why eSource makes sense today. Introduction to Electronic Source For Clinical Trial Sites Electronic Source,...
The impact of COVID-19 on clinical trials has likely become obvious for your site during this phase of the pandemic. Sites are struggling with screening holds, limited staff, an influx of sponsor requests while staff is not on-site, the challenge of retaining enrolled subjects, and more. It is now more important than ever to implement a business...
See exclusive survey data on what technologies clinical research sites are currently using, how much they’re spending, and why Electronic Source (eSource) and eRegulatory software is poised to break out in the clinical trials industry. Motivation for eSource and eRegulatory Survey Clinical Research IO (CRIO) was founded on the belief that we can get life-altering...
When a study coordinator uses eSource, he or she enters data into an electronic system like an electronic medical record or tablet computer, rather than onto paper. Data can then be transferred from the eSource system into the electronic case report (eCRF) system (also known as the electronic data capture (EDC) system), thus eliminating the...
