Riley Farley 
eRegulatory, often abbreviated as eReg or eReg/eISF (electronic investigator site file), refers to the use of electronic systems to manage regulatory documentation and compliance processes in clinical trials. eReg is an eClinical solution that streamlines the management of critical clinical trial documents. This safeguards that these important documents are securely stored, tracked, and accessed. Today, … Read more
A clinical research site’s study pipeline is tied to its overall performance, with CROs and sponsors rewarding sites that demonstrate efficiency, reliability, experience, and strong patient recruitment capabilities with more trial opportunities. Maintaining a strong and efficient study pipeline is critical for the success of any site. Having a well-managed pipeline ensures a steady flow … Read more
The evolution of data collection and management in clinical trials has seen a significant shift from traditional paper-based methods to electronic source (eSource). This transition has brought about profound changes in how clinical trials are conducted, driving increased data precision and staff efficiency, and the overall management of clinical trial data. Here, we dissect the … Read more
An interview with Phillip Stanford, Senior Director, Applications & PMO at EmVenio Research, a PCM Trials Company. Q: Can you tell us more about EmVenio Research’s business model and how it’s expanding research to underrepresented communities? A: EmVenio Research provides a scalable network of clinical trial sites. We are strategically located in clinical trial naïve … Read more
As clinical research organizations grow, many tasks can become siloed and the overall lack of transparency can lead to inefficiencies, delays, and increased costs. Standardizing study start-up and pipeline management is crucial for improving trial efficiency, ensuring regulatory compliance, and enhancing data quality. By implementing a centralized platform and establishing standardized operations across all site … Read more
This press release was initially published on Cision/PR Newswire. You can view the original release here. SAN ANTONIO, Texas, (July 16, 2024) – RealTime eClinical Solutions, a leading provider of innovative clinical trial management technology, is proud to announce its selection by one of the leading, top five global Contract Research Organizations (CROs) as a … Read more
Study start-up and pipeline management are fraught with challenges that can hinder progress and efficiency. These complex processes involve meticulous planning, coordination, and execution from all parts of a research site organization, leaving ample opportunity for delays. Despite advances in technology and methodologies, research teams continue to face significant challenges that can extend timelines and … Read more
Helios is a rapidly growing organization aiming to regularly add and onboard new sites. Unfortunately, their method for feasibility and other key processes have historically been site-based and lacked a cohesive, centralized plan. Additionally, their trial pipeline was highly individualized making it difficult for leadership to analyze, obscuring any potential trends and making processes hard to scale.
Tekton Research wanted to enable full remote monitoring and needed to be able to upload, manage, and share source documents with monitors and sponsors without redacting sensitive patient health information.
Velocity implemented the RealTime-Devana, previously PROPEL, software starting in March 2019 to centralize and automate workflows across the business development, feasibility, and all study start-up functions.
