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
The development of standards is a proven methodology for efficiency and quality. By implementing an eRegulatory solution, research institutions have the opportunity to standardize clinical trial documentation and processes.
Wow… 2020 has been a year of adaptation on a level that none of us could have predicted. As we celebrated last New Year’s Eve with the excitement of what 2020 would bring, none of us knew what we were in for! But here we are, proving that we are even more resilient than we … Read more
We explore Coastal Pediatric Research’s journey to adopting Complion’s eRegulatory solution which has enabled the site to increase efficiency, greatly improve time management, and eliminate duplication of work while conducting their clinical research studies. In the last post of this three-part series, we take a look at the training phase when adopting an eRegulatory solution.
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
We explore Coastal Pediatric Research’s journey to adopting Complion’s eRegulatory solution which has enabled the site to increase efficiency, greatly improve time management, and eliminate duplication of work while conducting their clinical research studies. In the second of this three-part series, we take a look at the implementation phase of the adoption of an eRegulatory solution.
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
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
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
The following except is taken from Scaling and Innovating: the Consolidation and Reinvention of Clinical Research Sites, an eBook courtesy of Clinical Research IO. Please click HERE to view the entire eBook. Barry Lake is the CEO and co-founder of Devana Solutions, a business analytics, startup and metrics capture solution for research sites and site … Read more