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eregulatory

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

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

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

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

3 Tips for Staying Audit-Ready

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3 Tips for Staying Aduit Ready

Maintaining audit-readiness is the best way to ensure that your site is prepared for audits and inspections, both planned and unplanned. This proactive approach prevents headaches and last-minute scrambling by staff in the event of an actual audit.  The following tips will help you ensure that your team is audit-ready. Create Create and establish an … Read more

FAQ: Compliance in Paperless Research Systems

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FAQ with Evelyn Jackson

Why does compliance matter when using an electronic system? Many established electronic systems provide research organizations a means to hold and secure valuable clinical research documents and data in a paperless environment that allow for greater site and sponsor efficiencies. These systems may include capabilities that span from recruitment tools, enrollment tracking, calendaring and appointment … Read more

5 Things to Look for in an eRegulatory System

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5 things with eRegulatory System

Due to increasing demand and shift to paperless research systems, it is vital to ask the right questions when searching for a site-based eRegulatory system. Sites can utilize eRegulatory systems to streamline regulatory processes, maximize cost-effectiveness, and make study information more accessible. These are some basic questions to ask when searching for an eRegualtory system. … Read more

Keeping research compliant amid the COVID-19 crisis

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Keeping research compliant

Many clinical research sites and sponsors are accepting new paperless processes in light of the novel COVID-19 crisis. With the inevitable switch to paperless clinical trial systems, one can hope that the same industry guidelines are equally enforced. With any process, there are rules; the clinical research process is no different with most prescription drugs … Read more

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