eDocs

Negotiating Sponsor Reimbursement for Site-based Technology​ – A Complete Guide for Clinical Research Sites

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Negotiating Sponsor Reimbursement for site-base technology: A complete guide for clinical research sites

Clinical research is undergoing a significant transformation, driven by the adoption of site-based electronic systems. As the industry shifts towards these advanced digital platforms, including virtual visits, telemedicine, and sophisticated data management systems, their value becomes increasingly evident. eClinical technologies are improving the efficiency of clinical trials and becoming integral to their success. Consequently, a growing … Read more

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

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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 In fact, since the FDA’s 2003 draft guidance on electronic technology in clinical investigations, the industry has witnessed a surge in the … Read more

Solutions for the Top 5 Pain Points for Clinical Research Sites 

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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

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

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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

Pros and Cons of e-Signatures in Clinical Research

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Pros and Cons of eSignatures in Clinical Research with CEO Rick GreenField Blog

As the clinical research industry moves into an increasingly paperless, electronic world, all stakeholders involved in clinical trial processes are faced with new workflows that include numerous benefits. However, in some cases, new challenges must be overcome. The move to electronic systems has been greatly accelerated due to Covid-19 as the need for contactless processes … Read more

3 Tips for Staying Audit-Ready

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3 Tips for Staying Aduit Ready

Maintaining audit-readiness is the best way to ensure that your site is prepared for audits and inspections, both planned and unplanned. This proactive approach prevents headaches and last-minute scrambling by staff in the event of an actual audit.  The following tips will help you ensure that your team is audit-ready. Create Create and establish an … Read more

Tips for getting sponsors to cover your site-based electronic systems

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Don't leave money on the table

With more and more research sites adopting site-based electronic systems, such as RealTime-eDOCS (eRegulatory) and RealTime-eSOURCE, it’s important for these sites to ask, “Am I leaving money on the table?”. Due to the value that these systems bring to the research process, it’s now more common than ever for sites to obtain payment from sponsors … Read more

Ask the Experts: Getting sponsors to cover your site-based electronic solutions

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Tips for getting sponsor to cover your site-based solutions

Site-based clinical trial software systems such as RealTime-eDOCS and eSOURCE are becoming more commonplace and essential than ever before.  These solutions are part of a fast-growing market of site-based systems in the research industry that is reshaping research processes. One common topic of concern of the sites is the cost of these systems and the … Read more

Segal Trials Announces eRegulatory Milestone with RealTime-eDOCS

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Segal Trials paperless with eDOCS

This June, Segal Trials announced their eRegulatory milestone with RealTime-eDOCS. “Congratulations to our Regulatory Department for going paperless! Electronic documents are safe, secure, and allow for quick and efficient handling of more complex studies- along with reducing our carbon footprint.”  – Segal Trials, LinkedIn Sites like those associated with Segal Trials experience numerous benefits when … Read more

Achieving Paperless Nirvana

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Paperless Nirvana Blog - RealTime-CTMS

Let’s face it, we have a paper problem. In a recent webinar, RealTime’s CEO, Rick Greenfield spoke about the existing “paper problem” in the clinical research industry and ways that we can overcome it to achieve “Paperless Nirvana”. As you already know, the Clinical Research Process primarily functions off of paper source documentation and manually … Read more