Year in Review, RealTime Software Solutions

Year in Review, RealTime Software Solutions

As we bid farewell to 2023, we take a moment to reflect on the incredible journey we’ve had at RealTime Software Solutions. This year has been marked by innovation, growth, and a steadfast commitment to advancing clinical trial management. Here’s a look at our year in review. Global Impact RealTime continues to make an impact … Read more

Expedite Your Study Startup – A Site Checklist

Study startup and site activation are key to the clinical trial process, but often suffer from delays. It can be a time-consuming undertaking and requires multiple teams and moving parts to successfully begin a trial at the best sites for the protocol. In fact, a recent ACRP survey revealed that study startup was ranked among … Read more

Speed Up Your Research Site Organization’s Turnaround Times 

Regardless of size and type, clinical research site organizations compete for trial opportunities from CROs and sponsors. There are many factors that can make a site stand out amongst the crowd, but turnaround times for key items may be one of the larger deciding factors. CROs and sponsors want to get trials up and running … Read more

Solutions for the Top 5 Pain Points for Clinical Research Sites 

Solutions for the top 5 pain points for clinical research sites

According to a review from the National Library of Medicine, clinical trials can fail for many reasons. Among the top five pain points include problems with (i) patient recruitment; (ii) enrollment; (iii) retention; (iv) safety issues; and (v) failing to maintain protocols or FDA guidance. However, from mitigating FDA audit risks to managing patient recruitment and engagement, there is … Read more

FDA Audit Readiness: How to Prepare & Share Faster with Monitors 

FDA Audit Readiness

In March 2023, the FDA issued an update to its Electronic Systems, Electronic Records, and Electronic Signatures in Clinical Investigations Questions and Answers Draft Guidance, reflecting the agency’s acknowledgement of the advancing use of electronic records, systems and signatures in clinical trials. Accordingly, clinical research sites face increasing pressure to demonstrate adherence to stringent industry … Read more

RealTime-eSource: Fueling 28x Revenue Growth at the University of the Sunshine Coast 

RealTime-eSource: Fueling 28x Revenue Growth at the University of the Sunshine Coast

Before partnering with RealTime, UniSC was grappling with huge piles of paper and operational inefficiencies that made it difficult to smoothly conduct multi-site decentralized trials for the rapidly expanding network. Using RealTime’s eSource, they were able to enforce protocol compliance, centralize source documents, eliminate paper workflows and reduce time on administrative tasks with streamlined workflows.

EmVenio Research Partners with RealTime Software Solutions

RealTime+EmVenio equals Increase Efficiency to Reach Diverse & Underserved Populations

EmVenio Research, a global network of mobile research sites providing localized trial access to diverse and underserved communities, today announced a strategic partnership with RealTime Software Solutions, LLC, a renowned provider of cutting-edge, digitally-optimized technologies designed for clinical research sites, CROs (clinical research organizations) and sponsors.

7 Secrets to Being Audit Ready at Any Time

Complion Inc. 7 Secrets to Being Audit Ready at Any Time

Are your clinical trials ready for an audit, inspection and/or site monitoring visit now?  If your organization is running clinical trials, you know that being audit ready is essential to meet Good Clinical Practice (GCP) guidelines, avoid trial delays and disruptions and, most importantly, to protect the rights and safety of human subjects. It’s also … Read more

Clinical Trial Audits, Monitor Visits, and Inspections: Understanding the Differences

Clinical Trial Audits, Monitor Visits, and Inspections (Oh My!): Understanding the Differences - blog graphic

Clinical trial inspections, monitoring visits, and audits are all important quality assurance measures that are used to ensure the integrity of clinical trials. However, there are some key differences between these three activities that are important for researchers to understand. By taking some time to learn more about them and how to prepare for them, … Read more

Streamline eRegulatory (eReg) Document Management with RealTime’s eDocs Solution for Clinical Trials

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