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Increasingly, clinical research sites are replacing traditional paper-based processes with Electronic Source (eSource) technology in clinical trials. The shift from paper-based processes to eSource represents a significant step forward in improving efficiency, accuracy, and compliance. As sites prepare to make the transition, whether from paper or an existing vendor, it is essential to understand the … Read more
Before partnering with RealTime, UniSC was grappling with huge piles of paper and operational inefficiencies that made it difficult to smoothly conduct multi-site decentralized trials for the rapidly expanding network. Using RealTime’s eSource, they were able to enforce protocol compliance, centralize source documents, eliminate paper workflows and reduce time on administrative tasks with streamlined workflows.
As new studies are coming up at your site, there is a lot to think about and prepare for. Getting studies set up in your CTMS for visit and financial tracking is one important process but building great source to drive excellent data collection processes is another major hurdle to being ready to execute. eSOURCE … Read more
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
RealTime-eSource is a cloud-based electronic source (eSource) data capture solution that effortlessly improves data accuracy and reduces protocol deviations. Request Demo Free Demo Sign documents electronically, no printing needed. Built-in checks help ensure data accuracy. Strict adherence to privacy and security regulations. Track data changes across time. Effortless Data Capture Streamline data collection, improve accuracy, … 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
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 Research Coordinators (CRCs) are the unsung heroes of clinical trials. They manage visits, communicate with participants, complete source data, handle sponsor queries, and keep everything moving, often across multiple studies at once. But with growing protocol complexity, tighter timelines, and more tech than ever, the job isn’t getting easier. That’s why a Clinical Trial … Read more
Clinical trials are fundamental in advancing medical science, offering new treatments and drugs to improve patient care. However, managing these trials is a complex task involving multiple stages and stakeholders. To streamline this process, Clinical Trial Management Systems (CTMS) have become essential for clinical research sites to organize efficient site management.