Networks are brick and mortar businesses by definition, but their differentiation lies in their ability to incorporate and optimize technology in every step of the workflow. No single technology vendor will be able to service the full gamut of needs. Instead, leadership teams should select and configure optimal solutions for different stages of the value...
The FDA routinely audits clinical research sites, and some of those sites happened to use CRIO eSource on the studies in question. With our broad reach and history as the leading site-adopted eSource solution, we have now established a database of audit results that prove what we’ve known intuitively: CRIO eSource reduces audit risks for...
Increased efficiencies Despite the myriad of additional issues caused by COVID, our study team’s efficiency dramatically increased with remote monitoring. I have long been a proponent of the potential of eSource and its advantages in clinical trials. From my experience as a CRA (Clinical Research Associate) I first wrote about eSource in November 2018, SOCRA...
Mary Brenner, MSN MArch RN, is CRIO’s Study Design Manager and brings deep-rooted expertise as a registered nurse to CRIO’s in-house study design team. In this quick Q&A, Mary shares the benefits of good study design for sponsors and sites, the downstream effects of standardized study designs, and gives tips for designing it on your...
BOSTON, MA – August 9, 2022 – CRIO, a Boston-based healthcare technology company streamlining clinical trials for sponsors, sites and patients, announced that it has reached another milestone, exceeding 2,000 clinical research sites standardizing on CRIO’s eSource platform. CRIO supports a variety of clinical trial data. To date, over 800 life science sponsors have data...
Clinical Research IO (CRIO)’s recent site survey showed that most sites have recovered business lost during the pandemic, are adjusting to the decentralized clinical trial model, and have implemented their own software in response. At the beginning of the pandemic, CRIO conducted a survey to look at the impact of coronavirus on research sites. By...
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...
Standard versus Custom Reports Every site has its own definition of success. As a clinical research site owner, manager, or medical director, you might be considering a deep dive into your analytics to guide decision-making and demonstrate progress to stakeholders. Sometimes, Standard Reports can get you just what you need. Standard Reports are report templates,...
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...
How did you get into research? I got started in clinical research as an undergrad. There was a group of physicians from Harvard that came to the University of Cincinnati, where I was studying, who started a centralized research office. I was part of that team. The first 2 years I coordinated, and my last...
Creating exceptional clinical research source documents is crucial for successful clinical trials. The best way to ensure that your source documents are ready is to know and understand the Clinical Study Protocol (CSP), which serves as the basis for your source documents. Use the CSP as your primary reference when creating source documents. This is...
