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Running a Study

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

It’s not about DCT – Diversity Driven Clinical Trials are the Key

ASK ME ANYTHING WITH JONATHAN ANDRUS Jonathan Andrus, President & COO at CRIO, is an active thought-leader and presenter in the life sciences industry. He serves on the board and executive committee of the Society for Clinical Data Management (SCDM) and is co-lead with the Decentralized Trials and Research Alliance (DTRA) workstream initiative. In this...

Running a Study

How the World’s Leading Vaccine Site Network Decreased Protocol Deviations by Almost 40%

Overview With 9 locations in Texas, California and Louisiana, Benchmark Research is the world’s leading vaccine network. Benchmark has performed over 10,000 studies on over 40,000 subjects and has received numerous awards, including being a five-time recipient of the Best Clinical Trial Site/Network award from the World Vaccine Congress. Challenge Historically, Benchmark used paper charts...

Running a Study

Direct Data Access versus Open API

Bala Nair is the Enterprise Architect at CRIO. With over 20 years of experience in the technology industry, Bala has shaped several cutting-edge engineering developments, from AOL’s Instant Messenger, to building software that delivered over 50% of video on demand content to U.S. households. At CRIO, Bala partners with other strategic owners to manage CRIO’s...

The CRIO Model 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...

Running a Study

Ask Me Anything – Hitting the Target with Good Study Design

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...

Running a Study

CRIO Innovation Theater: Creating an EMR to EDC pipeline through eSource

The CRIO Innovation Theater: Creating an EMR to EDC pipeline through eSource, presented insights to a jam-packed audience at DIA’s 2022 Global Annual Meeting. In case you missed it, view the recording right here, courtesy of DIA. Overview EMR-to-EDC integration is challenging to scale due to the fragmentation of health care providers. With EMR interoperability,...

Running a Study

eSource unlocks true remote monitoring benefits

Mark Joing is the Founder & CEO at Mojo Trials, a startup life sciences service provider delivering virtual site monitoring in clinical trials. He is also the Chief Operating and Financial Officer at Sanaby Health, a Special Purpose Acquisition Company created to accelerate innovation in healthcare. His 25+ year career in biopharma includes executive roles...

eSource makes the eCRF reliable Running a Study

eSource makes the eCRF reliable, accurate and timely

Bridging the gap eSource is the bridge between the protocol and the eCRF fields. To understand why, we need to understand what each does. The protocol describes the purpose of the study, the core hypotheses, the endpoints that are to be collected, and the resulting procedures to be performed to support those endpoints. The eCRF...

Running a Study

A Look into Alzheimer’s Research with Dr. Craig Curtis

How did you get into clinical research? During medical school, I completed several research externships and became very interested in research, but did not think of it as a career. After graduating and moving to Florida for residency, I met a local physician who was a principal investigator and owned a clinical research site.  We...

Running a Study

Make Virtual Monitoring Work for You: How eSource Can Help Sponsors Monitor Virtually During Covid-19

Striving for site success and business continuity amidst our global pandemic? Virtual monitoring bypasses the need for travel, made nearly impossible with the coronavirus, and becomes a critical technological solution for the kind of business continuity that keeps the industry reliable and strong. You can turn complexity into meaningful change. In this webinar, Raymond Nomizu,...