eSource vs EHR/EMR: Why Sites Use eSource for Clinical Trials 

eSource vs EHR/EMR: Why sites use eSource in clinical trials

The integration of technology in clinical trials increases accuracy, efficiency, and regulatory compliance. While both Electronic Health Records (EHRs) and electronic Source Data (eSource) systems are key components in this shift, they serve fundamentally different functions within the clinical trial process. What’s the difference? EHRs primarily focus on patient care and are intended for clinical workflows, whereas … Read more

eSOURCE Template Build Service with Nathan Levens

Learn more from Nathan Levens

RealTime-eSOURCE does the work for you and removes the burden of building source documents. Our system was built and tested by research site professionals, allowing more time to focus on subject recruitment, conducting study visits, and overseeing subject safety. One of the many services that RealTime offers to keep your staff’s focus on what really … Read more

Make the Switch in 2021 to RealTime-CTMS

Switch and save with RealTime CTMS

Say goodbye to 2020 and hello to fresh starts in 2021! RealTime-CTMS wants to help you get your year off to a great start and, perhaps it’s high time to re-evaluate your Clinical Trial Management System (CTMS). There is no better time to start your research than now. Choosing the right CTMS takes careful evaluation … Read more

FAQ: Compliance in Paperless Research Systems

FAQ with Evelyn Jackson

Why does compliance matter when using an electronic system? Many established electronic systems provide research organizations a means to hold and secure valuable clinical research documents and data in a paperless environment that allow for greater site and sponsor efficiencies. These systems may include capabilities that span from recruitment tools, enrollment tracking, calendaring and appointment … Read more

Keeping research compliant amid the COVID-19 crisis

Keeping research compliant

Many clinical research sites and sponsors are accepting new paperless processes in light of the novel COVID-19 crisis. With the inevitable switch to paperless clinical trial systems, one can hope that the same industry guidelines are equally enforced. With any process, there are rules; the clinical research process is no different with most prescription drugs … Read more

Utilizing Remote Monitoring Study Portals Through a Pandemic

Clinical research using motoring systems

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

ACRP 2019 – Key Takeaways (and Bandanas)

RealTime key takeaway from SCRS 2019

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

6 New Features of the RealTime-CTMS MobileAPP

Try our new mobileAPP

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

Behind the Software with Nathan Levens

Learn about Nathan Levens

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