Daenya McDonald 
This edition of RealTime Reports presents the findings from a survey of 255 clinical research professionals. The analysis reveals the current, site-level view of the real ROI of eSource.
Choosing the right trial site just got a lot smarter. RealTime eClinical Solutions and Inato have partnered to unite site performance data with patient access insights, giving sponsors and CROs unparalleled visibility into sites that are both high-performing and enrollment-ready.
About Shantell Gomez, eSource Build Specialist: Shantell Gomez is an experienced eSource Build Specialist with a background as a Clinical Research Coordinator in ophthalmology. With deep knowledge of site operations and years of hands-on form building across multiple therapeutic areas, she brings strategic insight, precision, and a user-first mindset to every project. Shantell also leads … Read more
With the federal government’s role as a major funding source for clinical research in question, at least in the near to mid-term, Academic Medical Centers are increasingly shifting their focus towards industry-sponsored research. Here’s how AMCs can leverage technology, like RealTime-Devana, to turn clinical research into a profitable enterprise.
Why the new RealTime? I am thrilled to share with you an exciting milestone in our company’s journey – a moment that marks the beginning of a new chapter for RealTime and our partner-clients across Complion and Devana Solutions. Our companies have experienced tremendous growth over the years, driven by our unwavering commitment to customer … Read more
At the center of every clinical trial lies a maze of regulatory requirements, from FDA regulations to institutional review board (IRB) approvals, and improving compliance in clinical trials remains an imperative. For academic medical centers (AMCs), ensuring compliance with these regulations can be an overwhelming task, often requiring extensive paperwork, meticulous documentation, and stringent adherence … Read more
Clinical research is undergoing a significant transformation, driven by the adoption of site-based electronic systems. As the industry shifts towards these advanced digital platforms, including virtual visits, telemedicine, and sophisticated data management systems, their value becomes increasingly evident. eClinical technologies are improving the efficiency of clinical trials and becoming integral to their success. Consequently, a growing … Read more
Amidst industry movements like the site network consolidation trend, broader diversity in clinical trials, and the increasing complexity of studies, clinical research sites are navigating an environment that demands even greater operational agility. RealTime Software Solutions recognizes this evolving need and offers a comprehensive eClinical suite of solutions designed to improve site operations, streamline workflows, … Read more
Clinical trials operate under a strict framework of regulations and compliance standards, reinforcing the importance of meticulous record-keeping. Well-documented cases such as Vioxx serve as reminders for clinical research sites and academic medical centers conducting clinical trials, highlighting the critical nature of maintaining impeccable organization and regulatory adherence. As the volume of data and documents … Read more
In an analysis published by Nature, nearly a quarter of all trials experienced setbacks due to strategic issues, commercial barriers, and operational challenges. The financial repercussions of such setbacks are significant, with drug developers facing potential losses ranging from $600,000 to $8 million per day. This statistic underscores the critical importance of effective, end-to-end clinical … Read more
