73% of sites reported using paper as the primary means of data collection In a 2018 CRIO site survey with over 100 respondents, sites reported that they use their Electronic Medical Record (EMR) primarily for patient recruitment purposes, but not for source data collection. 62% of site respondents reported that they use the EMR as...
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...
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.
Disclaimer: The examples noted in the following article are all firsthand accounts of the author, but for the purpose of this article have been combined into a single site visit. The visit depicted below is an aggregate of many sites and studies and is not necessarily an exact representation. The original version was written entirely...
Clinical Research IO‘s recent web survey found that COVID-19 is disrupting clinical research sites worldwide. The results are indicative of a significant slowdown in new drug development and long term effects on healthcare in general. 25% of sites have stopped recruiting Of the 75% that are continuing enrollment, about half (37%) are considering halting new...
In a survey commissioned by Clinical Research IO (CRIO), 62% of sites, who mainly conduct non-oncology trials, reported that they use their Electronic Medical Record (EMR) system as their primary system for recruiting patients, but only 13% reported that they use their EMR as their primary system for source data collection. For source data collection,...
While much of the research and development conducted by the global pharmaceutical industry relies on cutting-edge technology, one aspect of the process of developing and testing new drugs is decidedly low tech: clinical research. That’s what Raymond Nomizu, a Harvard-trained lawyer and former management consultant discovered when he decided to launch a company focusing on...
Most discussion about electronic source (eSource) documentation in the clinical research enterprise starts from a sponsor standpoint, with eSource being viewed as an extension-almost a mobile version of electronic data capture (EDC). In this view, sponsors provide sites with eSource systems that the sites use to collect data, which are then transmitted to the EDC...
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...
