During this challenging time, maintaining clinical trial progression is a novel challenge as on-site data and regulatory reviews are either impossible or extremely limited. Travel limitations and “stay home” initiatives across the country have hindered the way clinical trial data is handled. Many clinical research sites and sponsors are left without the data records needed … Read more
This June, Segal Trials announced their eRegulatory milestone with RealTime-eDOCS. “Congratulations to our Regulatory Department for going paperless! Electronic documents are safe, secure, and allow for quick and efficient handling of more complex studies- along with reducing our carbon footprint.” – Segal Trials, LinkedIn Sites like those associated with Segal Trials experience numerous benefits when … 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
As a clinical researcher, being at your desk to take care of study documentation, patient referrals and everything else that goes into managing your studies can be difficult and time-consuming. That’s why our team has created a mobile app that lets you access all your files, contacts, patient referrals, and inclusion/exclusion criteria on the go. … Read more
Research sites can now access popular eDOCS solution on mobile device with new app SAN ANTONIO—Want to access site eRegulatory files, sign documents with your thumb print, refer a patient to a study or look up site and sponsor contacts all on your mobile device? There’s an app for that! RealTime-CTMS launched the first-of-its-kind new … Read more
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
As of March 2024, there are almost 150,000 clinical studies registered in the United States,
