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clinical research

Running a Study

Progress Notes are Vital to Source Data

Progress notes are free-text entries by the investigator, coordinator or study team member that are inserted into the source record. Generally, these play a critical and highly undervalued role in the study process. Progress notes are often used to: Clarify or confirm any data points that may appear as outliers, even before a query is...

EMR to EDC - Nurse and doctor looking at computer screen Running a Study

EMR to EDC: Why sites and sponsors need CRIO’s EHR/EMR Integration

The new standard in clinical care Electronic Medical Records In the past several decades, Electronic Medical Records (EMR) have become standard in clinical care in the United States and many other countries, while Electronic Data Capture (EDC) systems have become standard in global pharmaceutical trials. Naturally, the industry has been highly focused on the tantalizing...

Running a Study

CRIO’s integrated eSource-EDC Model is a Game Changer

CRIO’s integrated eSource-EDC model revolutionizes both the data entry process at the site level and the monitoring process from the CRO perspective. According to a third party survey of CRAs who have used CRIO, CRAs agreed by a margin of 23:1 that this new model would increase overall trial efficiency, improve data quality, and enhance...

Running a Study

CRIO Reduces FDA Audit Risk by Over 70%

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...

Running a Study

The CRIO Model: How Monitoring and Data Management Transform Using eSource/EDC vs Traditional EDC

This document describes CRIO’s integrated eSource/EDC model, in which source data is collected electronically by the site using CRIO’s eSource system, then transmitted automatically to CRIO’s Reviewer module or to legacy EDC systems, which allows sponsors to review, query, code, lock and extract the data. This model unlocks significant savings for the sponsor/CRO, mainly by...

CRIO Company News

CRIO continues record growth in 2022, more than doubling the number of clinical research sites supporting over 800 life science sponsors

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...

CRIO Company News

CRIO Welcomes Jonathan Andrus as President & COO

Company Strengths Executive Management Team with Senior Industry Expert BOSTON, MA – April 19, 2022 – Clinical Research IO (CRIO), a Boston-based technology firm streamlining clinical trials for sponsors, sites, and patients, announced that Jonathan Andrus will join as President and Chief Operating Officer. Working collaboratively with the CRIO senior team, Andrus will focus on...