As technology evolves, so must we. We can’t settle for the same technology just because that’s the system we’ve always used. In our previous blog, “5 Things to Look for in an eRegulatory System,” we discussed what to look for in an eRegulatory system for clinical trial management. User experience, a monitoring portal, secure centralized … Read more
As new studies are coming up at your site, there is a lot to think about and prepare for. Getting studies set up in your CTMS for visit and financial tracking is one important process but building great source to drive excellent data collection processes is another major hurdle to being ready to execute. eSOURCE … Read more
Customers are the heart of RealTime-CTMS and each day our team strives to provide outstanding customer support to all of our clients. Joining RealTime in 2018, Norma Zayas leads the charge as our Success Team Manager, bringing a strong background in account management and client relations. Norma manages our team of dedicated support specialists ready … Read more
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
Say goodbye to 2020 and hello to fresh starts in 2021! RealTime-CTMS wants to help you get your year off to a great start and, perhaps it’s high time to re-evaluate your Clinical Trial Management System (CTMS). There is no better time to start your research than now. Choosing the right CTMS takes careful evaluation … Read more
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
With clinical trials in full swing, researchers around the globe are bustling with work. Halted or paused trials are beginning to resume, and COVID-19 research efforts have heavily contributed to our industry’s workload. Luckily, we live in an age where software has eased the workload for all parties in the pharmaceutical and research industry. RealTime … Read more
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.
This October, RealTime Software Solutions is proud to partake in SCRS Virtual Global Site Solutions Summit! With a full virtual events and workshops schedule, we wanted to share the sessions we are most excited about. Tuesday, October 6, 2020 | 2:45 – 3:45 EST Site Business Health: Withstanding Disruption During a Pandemic Many clinical research … Read more
