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
At RealTime, our mission is to strive for the complete success of our customers every day. By accomplishing this, we have dedicated our time to finding strong individuals to help shape tomorrow’s clinical trial software. RealTime is dedicated to providing exceptional support, which is why we search for team members above and beyond our customers. … Read more
Choosing the right Clinical Trial Management System (CTMS) takes careful evaluation requiring a substantial time investment as well as extensive research. When choosing a CTMS, you should feel confident that you are making the right decision, as the wrong decision can be very costly to your organization in the short-term, resulting in long-term consequences. The Depth … Read more
Why does compliance matter when using an electronic system? Many established electronic systems provide research organizations a means to hold and secure valuable clinical research documents and data in a paperless environment that allow for greater site and sponsor efficiencies. These systems may include capabilities that span from recruitment tools, enrollment tracking, calendaring and appointment … Read more
Many clinical research sites and sponsors are accepting new paperless processes in light of the novel COVID-19 crisis. With the inevitable switch to paperless clinical trial systems, one can hope that the same industry guidelines are equally enforced. With any process, there are rules; the clinical research process is no different with most prescription drugs … Read more
During this challenging time, maintaining clinical trial progression is a novel challenge as on-site data and regulatory reviews are either impossible or extremely limited. Travel limitations and “stay home” initiatives across the country have hindered the way clinical trial data is handled. Many clinical research sites and sponsors are left without the data records needed … Read more
The year is 2020 – you’re running a clinical research site and realize your workflow is still primarily running off paper systems. Files are overflowing your workspace, paperwork is getting lost between your site staff and doctors, and before you know it, you’re stuck in a paper vortex! Has this ever happened to you? The … Read more
Patient recruitment in clinical trials is undeniably one of the most challenging obstacles facing the clinical research industry. The lack of patient participation in clinical trials can be due to multiple factors but the most likely cause of low or slow enrollment is simply the lack of clinical trial awareness. Digital technology and connectivity have … Read more
Building a strong team is crucial to the success of our customers. At RealTime, we have dedicated our time to finding strong individuals to help shape the clinical trial software of tomorrow. Our goal is to give back to clinical researchers by creating software that is more efficient, reliable, and easy to use, while providing … Read more
RealTime Software Solutions Announces They Have Joined SCRS Global Impact Partner Program As a leader in clinical trial software, RealTime hopes to benefit sites, sponsors and CROs through a new partnership with SCRS. As a dedicated leader in the clinical trial industry, RealTime Software Solutions is pleased to announce that they have joined the Society … 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.
At the center of every clinical trial lies a maze of regulatory requirements, from FDA
Clinical research is undergoing a significant transformation, driven by the adoption of site-based electronic systems.
Amidst industry movements like the site network consolidation trend, broader diversity in clinical trials, and
Clinical trials operate under a strict framework of regulations and compliance standards, reinforcing the importance
