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.
The Journal of the Society for Clinical Data Management (JSCDM) recently published the original research article “Comparison of electronic health records and electronic source data in clinical research trials: a retrospective review” which was co-authored by Amelia Tian, CRIO Solutions Consultant, and Olivia Dennis, CRIO Analytics and Data Migration Manager, alongside Dr. Elena Christofides (Endocrinology...
Compliance Update: The 21 CFR Part 11 Regulation is a cornerstone of conducting clinical trials in today’s world. The release of the regulation 1997 established guidelines for the use of electronic records and electronic signatures in FDA-regulated industries and had a significant impact on the pharmaceutical and medical device industries. The FDA began working on...
We talked to Takoda Rolland, a Clinical Team Manager (CTM) from a Contract Research Organization (CRO), to learn about their experience implementing CRIO for remote monitoring on a large, global clinical trial. Question: How did you start using CRIO for remote monitoring as a CRO? I have long been a proponent of the potential of...
