Large-scale research data can seem overwhelming in a data-driven industry. While managing a multi-site or extensive site network, centralizing processes and taking advantage of multiple resources across the network is the goal, but few systems on the market can truly bring this level of efficiency to a site network. Aggregating data and providing valuable network-wide … 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
Clinical research technology is constantly changing. Which is why we have dedicated our time to finding strong individuals to help shape the clinical trial software of tomorrow. Our goal as a team is to give back to clinical researchers by creating software that is more efficient, reliable, and easy to use. This month, we feature … Read more
Whether you are looking for a better electronic data management solution for your site, or you are just in the information gathering stages, RealTime’s eSOURCE solution makes working anywhere in a clinical trial site setting possible. RealTime is a leader in the industry of advanced research information systems offering solutions from CTMS, eDOCS, SitePAY, GlobalPAY, … Read more
RealTime Software Solutions’ Success Team is compiled of talented individuals dedicated to providing the best support for RealTime customers. This month, we are highlighting an exceptional team member and manager who goes above and beyond for RealTime customers. Norma Zayas joined the RealTime organization in 2018. With a strong background in account management and client … Read more
Each year, RealTime attends a variety of conferences around the globe in hopes of aiding clinical research professionals, sites, sponsors and CROs on their paperless journey. RealTime attended ACRP in Nashville, Tennessee this April and the team had the opportunity to network with professionals in the industry while gaining insight into the realm of clinical research … Read more
From text messages to video conference calls, mobile devices have become part of an everyday routine. Consequently, mobile device usage has become more evident in the clinical research setting. Utilizing electronic devices can improve efficiency and streamline research data across your site. Implementing the right mobile software can drastically enhance the study process. The new … Read more
Our goal as a team is to give back to clinical researchers by creating software that is more efficient, reliable, and easy to use. This month, we are featuring a team member that has gone above and beyond for our customers, Nathan Levens. Nathan has over 10 years’ experience in the clinical research industry. He … 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
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
RealTime eClinical Solutions is a leading, enterprise-grade technology provider facilitating global clinical trials with a comprehensive eClinical platform. Purpose-built for clinical research sites, site networks, academic medical centers, sponsors, and CROs, the platform goes beyond traditional CTMS to empower research and business workflows for modern-day clinical trials.
At the center of every clinical trial lies a maze of regulatory requirements, from FDA
Clinical research is undergoing a significant transformation, driven by the adoption of site-based electronic systems.
Amidst industry movements like the site network consolidation trend, broader diversity in clinical trials, and
Clinical trials operate under a strict framework of regulations and compliance standards, reinforcing the importance
