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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

RealTime Software Solutions Reports Record Growth in 2023, Emerging as the Premier Clinical Trial Management Solution for Clinical Research Sites 

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RealTime reports record growth

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

Clinical Trial Site Management: A Complete Checklist for Clinical Research Sites

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Clinical Trial Site Management

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

Streamline eRegulatory (eReg) Document Management with RealTime’s eDocs Solution for Clinical Trials

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In the ever-evolving field of clinical research, technological advancements continue to revolutionize how we conduct studies and collect data. One such innovation is the Realtime-eDOCS solution, a game-changer for clinical research sites. In this blog post, we will explore the benefits this eRegulatory (eReg) solution brings to these sites and how it can enhance their … Read more

Secrets to Becoming a Top Recruiter for Clinical Research Studies

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According to the National Library of Medicine, an estimated 80% of trials fail to meet enrollment deadlines resulting in recruitment extensions and even termination of studies. If you are a clinical research site owner, this is most likely not a surprise. What you may not know is that this doesn’t have to be a significant problem. … Read more

Do you REALLY own your CTMS data?

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As clinical research sites and site networks become more sophisticated, they’ve come to rely heavily on advanced CTMS, eRegulatory and eSOURCE solutions to manage their full set of clinical operations. The size and complexity of data stored in these systems often includes HIPAA protected subject demographic data, medical and medication history, study-specific enrollment data, financial … 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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Website by ImageBloom website design clinical research and medical industry marketing services