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

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 

The Benefits of eRegulatory for Academic Medical Centers

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 professionals.

Advancing Clinical Trial Site Management: Strategies for Improved Performance

Advancing Clinical Trial Site Management: Strategies for Improved Performance

One common frustration in the initiation phase of clinical trials is the frequent occurrence of delays. 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 … Read more

Going Digital in Clinical Trials with Electronic Delegation of Authority, eSignatures, and Audit Trails

Going Digital in Clinical Trials with Electronic Delegation of Authority, eSignatures, and Audit Trails

The adoption of digital solutions is becoming commonplace due to the increased efficiencies of electronic solutions in maintaining compliance in clinical trials. In this blog post, we’ll explore the critical components of going digital with electronic delegation of authority, electronic signatures (eSignatures), and audit trails – and how they are safeguarding compliance and patient safety … Read more

Save Our Sites LinkedIn Live: How Is RealTime Working To Save Our Sites?

Save Our Sites LinkedIn Live: How is RealTime Working to Save Our Sites?

In this Save Our Sites LinkedIn Live – How is RealTime Working to Save Our Sites, the organizers of the upcoming Save our Sites conference, caught up with the founders of RealTime, Complion, and Devana Solutions. They discussed how their strategic partnership is reshaping technology in the clinical research landscape. The amalgamation of RealTime, Complion, and Devana signifies a move to consolidate all … Read more

Save Our Sites LinkedIn Live – How Will RealTime Save Our Sites?

Save our sites linkedin live

Built for sites by a site owner, RealTime Software Solutions is designed to help sites overcome some of the top challenges that they’ll face in 2024. In this Save Our Sites LinkedIn Live – How is RealTime Working to Save Our Sites, the organizers of the upcoming Save our Sites conference, caught up with the founders of … Read more

Leading Pediatric Research Center Selects  Complion eRegulatory Platform

Complion eRegulatory platform

SAN ANTONIO, Texas, Jan. 23, 2024 – Complion, LLC, a leader in eRegulatory solutions (eReg and eISF) for clinical trials, is teaming up with a world-renowned pediatric research center. This collaboration signifies a notable achievement for Complion, a RealTime Software Solutions Company, as this esteemed pediatric research center adopts their enterprise-grade eRegulatory platform to ensure … Read more

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

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

Why Your Clinical Research Site Needs More Than a CTMS

Clinical trials require precise management across various domains such as patient recruitment, data collection, regulatory compliance, and stakeholder communication. While Clinical Trial Management Systems (CTMS) have been pivotal in organizing and simplifying many of these aspects for clinical research sites, the complexity of modern clinical research often necessitates a broader array of solutions.   CTMS platforms … Read more

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

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