eSOURCE Template Build Service with Nathan Levens

Learn more from Nathan Levens

RealTime-eSOURCE does the work for you and removes the burden of building source documents. Our system was built and tested by research site professionals, allowing more time to focus on subject recruitment, conducting study visits, and overseeing subject safety. One of the many services that RealTime offers to keep your staff’s focus on what really … Read more

The Power of CTMS Website Integration

Why your CTMS needs website capabilities

Managing your website and keeping it up to date is already a painstaking process but managing your study listings on your website can be even more time-consuming and costly. This is especially true if you pay a website management company to add/remove studies for you.  The good news? RealTime-CTMS has an option to link your … Read more

3 Tips for Staying Audit-Ready

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

The Case for Standards in Site Regulatory

Site regulatory standards

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.

Transition and Adaptation of Clinical Research in 2020

A letter from Rick Greenfield

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

Part 3: How Coastal Pediatric Trained Staff on an eRegulatory Solution

Training on an eRegulatory Solution

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.

Why it’s important to choose the right CTMS the first time

Choosing the right CTMS

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

Part 2: How Coastal Pediatric Implemented an eRegulatory Solution

How Coastal Pediatric implemented an eRegulatory solution

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.

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

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

Behind the Software with Shannon Samuel

Learn more about Shannon Samuel

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

Access the Report

Complete the form below to access the full report.