How electronic data is streamlining clinical research. Major advancements in technology and cutting-edge software are drastically improving and reconstructing the way research is conducted. The collection of accurate data and information is providing a new perspective on the industry. So, how can electronic data simplify the research process? Let’s break it down. Accuracy in data … Read more
Let’s face it, we have a paper problem. In a recent webinar, RealTime’s CEO, Rick Greenfield spoke about the existing “paper problem” in the clinical research industry and ways that we can overcome it to achieve “Paperless Nirvana”. As you already know, the Clinical Research Process primarily functions off of paper source documentation and manually … Read more
You have probably heard the term S.O.M.S., but what does it mean? Quite simply, SOMS stands for Site Operations Management System. It rhymes with Tom’s… it’s SOMS! OK, now you can say it, but what is it? In the vast arena of software available for clinical research sites, there is a lot to navigate and … Read more
The clinical research industry has inevitably been slow to adopt technological advances primarily due to regulatory constraints and a fear of change that could disrupt current processes. While the regulatory guidance has been issued by the FDA, development of solutions that can conform to the guidance AND improve efficiency is challenging. In the recent years, … Read more
Clinical trials operate under a strict framework of regulations and compliance standards, reinforcing the importance
In an analysis published by Nature, nearly a quarter of all trials experienced setbacks due
Increasingly, clinical research sites are replacing traditional paper-based processes with Electronic Source (eSource) technology in
SAN ANTONIO, Texas, March 26, 2024 — Complion, LLC, a wholly owned subsidiary of RealTime
