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 is proud to offer many timesaving solutions for researchers everywhere. Here is a more in-depth look into these timesaving solutions!
DecenTRIAL
RealTime-DecenTRIAL is a new way for Sponsors and CROs to manage clinical trials centrally. RealTime-DecenTRIAL allows complete connectivity and real-time remote monitoring for sites while delivering world-class eSource and eRegulatory systems for rapid data and document collection. DecenTRIAL also supports virtual visits and will soon have eCONSENT built in for even greater convenience.
CTMS
Keeping up with your trials at the site-level can be a headache. RealTime-CTMS has many built-in features that can cut down on time and costs. An example of this is the financial and accounting tracking tools built within the CTMS. Simply generate study financial reports with the click of a button to show all accrued revenues and expenses as well as receivables and payables. The team at RealTime also offers financial study template building services that can save site staff a ton of time!
eSOURCE
Is managing source data and documents taking more time than it should? With Realtime-eSOURCE, you can save time on data collection, management and monitoring with customized source templates and an advanced monitoring portal! Custom source templates allow you to reuse and modify form templates for future studies. You can also standardize your source documents across all studies to promote compliance and efficiency. Let’s face it; mistakes happen, which is why RealTime-eSOURCE leverages built-in data parameters to ensure accuracy and completion.
eDOCS
Are you struggling to manage all your eRegulatory processes? We know the struggle. RealTime-eDOCS offers a seamless platform where you can manage eRegulatory records while maintaining inspection readiness. RealTime-eDOCS allows researchers to e-sign documents from virtually anywhere. No more chasing down doctors for signatures! The eDOCS cart lets you group documents for easy sharing and bulk signing. eDOCS is also Part-11 and HIPAA compliant, so you can rest easy knowing that your data is safe, protected and compliant.
So, are you ready to try out these timesaving products? Give us a call, and our team will take you on a complete tour of these solutions and their innovative features. Schedule a FREE DEMO by calling (210) 852-4310 or fill out the form below.
