Daenya McDonald 
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. Historically, clinical trial management … Read more
Technological advancements and adoption in clinical trials continue to reshape the way data is collected, managed, and analyzed by clinical research sites, sponsors and CROs. Over the last decade, Electronic Source (eSource) has gained prominence for enabling direct data entry by investigators, reducing transcription errors and enhancing data quality. eSource in clinical trials is often … Read more
Built for sites by a site owner, RealTime Software Solutions is designed to help sites overcome some of the top challenges that they’ll face in 2024. In this Save Our Sites LinkedIn Live – How is RealTime Working to Save Our Sites, the organizers of the upcoming Save our Sites conference, caught up with the founders of … Read more
SAN ANTONIO, Texas, Jan. 23, 2024 – Complion, LLC, a leader in eRegulatory solutions (eReg and eISF) for clinical trials, is teaming up with a world-renowned pediatric research center. This collaboration signifies a notable achievement for Complion, a RealTime Software Solutions Company, as this esteemed pediatric research center adopts their enterprise-grade eRegulatory platform to ensure … Read more
SAN ANTONIO, Texas, Jan.17, 2024 – RealTime Software Solutions, a leading provider of cutting-edge eClinical solutions for clinical research sites, proudly announces a year of remarkable growth and success in 2023, solidifying its position as the premier choice for clinical research sites navigating the complexities of clinical trials. The company’s success has been amplified through … Read more
Do you have the right site technology to start studies faster, reduce FDA audit risk and lower protocol deviations? Increasingly, clinical research is transitioning from paper-based processes to the adoption of electronic workflows. In fact, since the FDA’s 2003 draft guidance on electronic technology in clinical investigations, the industry has witnessed a surge in the … Read more
As we bid farewell to 2023, we take a moment to reflect on the incredible journey we’ve had at RealTime Software Solutions. This year has been marked by innovation, growth, and a steadfast commitment to advancing clinical trial management. Here’s a look at our year in review. Global Impact RealTime continues to make an impact … Read more
According to a review from the National Library of Medicine, clinical trials can fail for many reasons. Among the top five pain points include problems with (i) patient recruitment; (ii) enrollment; (iii) retention; (iv) safety issues; and (v) failing to maintain protocols or FDA guidance. However, from mitigating FDA audit risks to managing patient recruitment and engagement, there is … 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.
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
