Daenya McDonald 
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
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
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.
