Insights on clinical research written by CRIO
Discover our latest eBook, “The Rise of the Clinical Trial Site Mega Network” the third installment in our “Scaling and Innovating” series. The first book in this series was published in 2019, where CRIO predicted that clinical research site networks would continue to grow and consolidate the industry. The second eBook, which was published in...
In the past several decades, Electronic Health Record (EHR) systems have become the standard in documenting 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 possibility of integrating EHR into EDC....
In a comparison of EMR and eSource data, we analyzed the medications and medical history documented in the EMR versus the EDC of subjects in active ongoing clinical research studies. The goal was to assess the validity of the assumption of the utility of using EMR data directly. The present study reveals a significant data...
You need a partner that is capable of meeting your enterprise requirements and regulatory obligations. CRIO is an enterprise-grade eClinical solution. This guide describes some of CRIO’s best practices that differentiate us from other vendors. Download the full white paper to explore CRIO, the industry’s #1 site-based eSource solution.
With nine locations in Texas, California and Louisiana, and five-time recipient of the Best Clinical Trials Site/Network award from the World Vaccine Congress, Benchmark Research is one of the industry’s leading vaccine network. This white paper provides an in-depth analysis from three participating Benchmark Research. Specifically, results indicate that using CRIO electronic source (eSource) reduces...
This primer describes CRIO’s integrated eSource-EDC model. In this model, data are captured once by the site, against electronic source templates built by the sponsors. Next, the data are surfaced in a sponsor-facing application called Reviewer EDC. Using Reviewer EDC, sponsors can review, query, lock, code, and extract the data. Download the full case study...
In a 2019 CRIO eBook, “Scaling and Innovating: The Consolidation and Reinvention of Clinical Research Sites,” we explored the emerging trend of clinical research site consolidation. Today, there are five times as many site networks today as in 2015. Sponsors are taking notice and driving a lot of this shift. What does this mean for...
A pack of 5 detailed SOP templates for your clinical trial site during the Coronavirus (COVID-19) Outbreak.
Identifying ways to increase efficiency in the clinical research workforce. Staffing shortages at clinical research sites are having a major impact on clinical trials worldwide. Exacerbated by the COVID-19 pandemic, these workforce constraints have forced research professionals to accomplish more with fewer resources. CRIO and TPS surveyed members of the Association of Clinical Research Professionals...
This CRIO white paper, A Survey of Clinical Research Site Operations Post COVID, includes the complete results from CRIO’s latest web survey on post-COVID operations at clinical research sites.
Choosing the right eSource solution is a critical decision for clinical research sites because it can significantly impact operational efficiency, data quality, and compliance. With numerous options available, selecting the right eSource system can be a daunting task. To simplify the process, it is important to consider several key factors. We’ve compiled a comprehensive checklist...
The clinical research industry made big changes to adapt to the operational disruptions of a global pandemic. Today, it’s more exciting and diverse than ever before. With the high level of recent technology adoption, CRIO wanted to learn more about CRA experiences using the CRIO platform. Method Between March 16 and March 30, 2022, a...
