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Daenya McDonald

Improving Clinical Trial Compliance: Top 5 eRegulatory Features for Academic Medical Centers  

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Improving compliance in clinical trials

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

Negotiating Sponsor Reimbursement for Site-based Technology​ – A Complete Guide for Clinical Research Sites

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Negotiating Sponsor ReimbursEment for Site-based Technology​ - A Complete Guide for Clinical Research Sites

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

Data Migration: Getting Started with RealTime  Software Solutions 

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Data Migration: Getting Started with RealTime Software Solutions

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 Trial Naming Conventions: Refining Standards in Clinical Trial Management 

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Clinical Trial Naming Conventions

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

Maximizing Budgets in Clinical Trials: The Financial Advantages of an Integrated eClinical Solution  

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Maximizing Budgets in Clinical Trials

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

How to Implement eSource – A Guide for Clinical Research Sites

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How to implement esource

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

Premier Pediatric Research Center Adopts Complion’s eISF Platform to Strengthen Pediatric Research Excellence  

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Pediatric Research Center Adopts Complion’s eISF

SAN ANTONIO, Texas, March 26, 2024 — Complion, LLC, a wholly owned subsidiary of RealTime Software Solutions, LLC and a leader in eRegulatory solutions, proudly announces the latest adoption of its eRegulatory/eISF solutions by a leading, not-for-profit pediatric hospital and active research facility. This collaboration marks a significant milestone, as another of the nation’s top … Read more

The Benefits of eRegulatory for Academic Medical Centers 

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Principal Investigator holding a tablet

As of March 2024, there are almost 150,000 clinical studies registered in the United States, with Academic Medical Centers (AMCs) overseeing a staggering volume of clinical trials annually across various therapeutic areas. At the forefront of medical innovation, patient care, and medical education, AMCs drive advancements in healthcare while nurturing the next generation of medical … Read more

Improving Patient Engagement & Retention Strategies with ENGAGE!  

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Improving Patient Engagement & Retention Strategies

Maintaining patient engagement and minimizing dropout rates in clinical trials is a persistent hurdle, with dropout rates soaring up to 30% in some studies. The National Institutes of Health underscores the importance of building trust, engaging communities, and ensuring clear and culturally sensitive communication at every stage, from pre-recruitment planning to post-study dissemination of results. … Read more

Behind the Software: Becoming a Great Place to Work 

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Great place to work

RealTime has always believed that our people are our greatest asset. We are thrilled to announce that our commitment to fostering a positive and inclusive workplace culture has been recognized once again by a Great Place to Work® Certification! In this issue of Behind the Software: Becoming a Great Place to Work, we’re spotlighting the culture … Read more

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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.

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