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 10 pediatric research institutions has chosen Complion’s sophisticated eISF system to improve compliance and data management processes across its research endeavors.
As a leading pediatric medical center overseeing almost 150 ongoing studies across its research portfolios, this world-class institution sought an exceptional eClinical solution to meet the demands of its complex pediatric clinical research. Complion was chosen because of its ability to simplify research workflows by converting manual, time-consuming tasks into automated, efficient operations. This selection highlights Complion’s focus on advancing clinical trial management, optimizing processes, and reducing administrative staff workloads.
“We are thrilled to see leading pediatric medical centers adopting our platform. Our team uniquely understands the challenges that they’re facing in compliance, and we’re thrilled that Complion is becoming the premiere choice,” states Rick Arlow, president and founder at Complion. Institutions that have already adopted Complion report a fivefold increase in inspection readiness, a 75% reduction in monitoring interactions, and double the rate of study start-ups for sites, sponsors, and CROs.”
Complion’s eISF system is distinguished by its targeted design, developed to meet the unique requirements of complex pediatric clinical research. Its user-friendly interface and robust capabilities make it an increasingly preferred choice for research and academic medical centers aiming to streamline their regulatory documentation and enhance operational efficiency.
About RealTime Software Solutions:
RealTime Software Solutions, LLC stands at the forefront of the industry as a premier provider of cutting-edge eClinical solutions tailored to the needs of clinical research sites, site networks, sponsors, and CROs. Our comprehensive suite of products includes the Clinical Trial Management System (CTMS), eRegulatory document management (eDocs), electronic data capture for source documents (eSource), participant payments (SitePay/GlobalPay), participant engagement solutions (Text, eConsent, and MyStudyManager™ Participant Portal), Complion eRegulatory/eISF, and Devana for pipeline management, study start-up, and business intelligence.
With a proven track record of empowering research organizations, we are committed to delivering innovative, user-friendly interfaces that redefine clinical research for clinical trials. Through our solutions, we aim to revolutionize how research is conducted, providing unparalleled efficiency and effectiveness at every stage of the process.
