Riley Farley 
Sponsors are raising their expectations for clinical research sites to deliver higher levels of efficiency, data integrity, compliance, and patient engagement. With advancements in eClinical technology, increasing regulatory demands, and a growing focus on diversity and hybrid trials, the bar for site performance has never been higher. Several key trends are shaping these expectations. From … Read more
With the year winding down, it’s impossible not to pause and feel a sense of pride in all that we’ve accomplished together at RealTime eClinical Solutions. 2024 has been marked by a brand refresh, stronger partner collaboration, and a continued commitment to empowering the clinical research community and advancing clinical research together. Before we turn … Read more
At the recent Decentralized Trials & Research Alliance (DTRA) conference, industry leaders took to the center stage to discuss one of the most pressing challenges in clinical research: reducing site burden and improving operational efficiency. With the complexity of clinical trials growing exponentially – sites now juggle an average of 22 systems per study – … Read more
Electronic Source (eSource) presents a compelling case for reducing monitoring costs in clinical trials. By streamlining data collection, improving accuracy, enabling remote monitoring, strengthening compliance, and altogether reducing administrative burdens, eSource solutions provide a powerful tool for clinical research sites, sponsors, and CROs looking to achieve better outcomes. There’s a reason why thousands of sites … Read more
This webinar served as a call to action for the industry, emphasizing the need for collaboration, transparency, and innovation to make clinical research a more inclusive and effective care option.
Clinical research is highly competitive and regulated. Staying on top of study oversight and management is crucial for research sites aiming to run efficient, compliant, and impactful trials. But with many moving parts – including study start-up, patient recruitment, compliance tracking, and more – managing numerous trials across multiple locations can become overwhelming. For many … Read more
This press release was initially published on Cision/PR Newswire. You can view the original release here. SAN ANTONIO, TX – November 12, 2024 – RealTime eClinical Solutions, a leader in cloud-based software for the clinical research industry, is proud to announce the expansion of its Professional Services, designed to help clinical research sites, AMCs, sponsors, … Read more
Before adopting RealTime’s comprehensive eClinical solutions, CHR encountered several challenges using multiple systems from different vendors related to fragmented systems and workflows. Reporting delays were a significant issue, as pulling reports from multiple systems required downloading separate data sets, reconciling them, and aligning information due to inconsistent naming conventions.
The adoption of eReg/eISF solutions in clinical trials can significantly improve outcomes across Academic Medical Centers (AMCs) and health networks, where efficient regulatory documentation management is essential. eReg/eISF solutions, electronic platforms specifically designed for regulatory document and process management in clinical trials, streamline the entire workflow, from document creation and secure storage to real-time access … Read more
The Irving Aging Well Expo in September 2024 drew over 2,000 attendees eager to learn about the latest in health and wellness, and Cedar Health Research (CHR) emerged as a standout participant. Leveraging a revamped patient recruitment strategy and the industry’s most comprehensive eClinical technology, CHR demonstrated how innovation and a fully integrated platform could … Read more
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.
