Maximize Growth And Profitability With These Powerful Metrics
Monitoring Key Performance Indicators (KPIs) is essential to ensuring the profitability and growth potential of your clinical research site.
Solutions
Devana Solutions Connects Research Operations and Business Intelligence at Scale with Clinical Conductor Integration
A new interface between Devana’s IGNITE and PROPEL products and Advarra’s Cloud-Based Clinical Trial Management System establishes an end-to-end solution for efficient research conduct and world-class business intelligence. CHAPEL HILL, NC (March 10, 2022) – Devana Solutions is pleased to announce a new, at scale CTMS- integration solution for research organizations utilizing Advarra’s Clinical Conductor … Read more
Accel Research Sites makes clinical trials more accessible with Devana Solutions’ PROPEL platform
Chapel Hill (February 22, 2022) – Accel Research Sites is bringing clinical trials to even more patients, right where they live and work, thanks to an industry-leading clinical trial platform from Devana Solutions. Accel is the latest clinical trial network to convert to Devana’s PROPEL Enterprise Platform, which will help the organization connect central teams … Read more
5 Crucial Considerations for Selecting a CTMS
With a clinical trial management system (CTMS), you can more efficiently manage the day-to-day operations of running a clinical trial as well as easily organize trial data in one central location. Learn what to consider when selecting a CTMS.
How a Mobile App Improves Site Clinical Trial Performance
Does your CTMS system have a dedicated mobile app? If not, you may be asking, “Why would I even need a CTMS mobile app? My current CTMS vendor claims that it is not necessary because my CTMS scales to mobile devices.” Let’s dive into how RealTime, the only CTMS company to have a dedicated mobile app, is enabling clinical research coordinators, investigators, and other front-line researchers to execute their daily tasks more efficiently and effectively using tools that are only possible with a mobile app. The following are some of the key benefits that RealTime customers can enjoy by using the features on our MobileApp:
Devana Brings Cloud-Based Collaboration to Clinical Trial Central Research Teams
The pandemic has had a significant impact on the clinical research industry. In response to the COVID-19 pandemic, regulatory authorities have been calling for an increased adoption of decentralized clinical trials (DCTs). Devana Solutions has been pivotal during this time, helping central research operations teams collaborate safely and remotely on our platform and connect to … Read more
New Customer Feature Request Form Brings Ideas to Life
At RealTime, we are constantly investing in technology improvements to ensure customers get the most out of RealTime solutions. We take our customer’s input seriously and use it to make sure our solutions meet their needs. In fact, most of our updates have originated directly from the voice of our customers! In an effort to … Read more
Data Analytics & Making Decisions for Better Outcomes
At Devana Solutions, our motto is Better Data, Better Decisions, Better Outcomes. But what exactly does that mean to us—and for you? Let’s take a look at how superior data analytics can make a huge impact on the clinical trial industry as a whole—and your organization in particular. Better Data We believe complete data … Read more
Pros and Cons of e-Signatures in Clinical Research
As the clinical research industry moves into an increasingly paperless, electronic world, all stakeholders involved in clinical trial processes are faced with new workflows that include numerous benefits. However, in some cases, new challenges must be overcome. The move to electronic systems has been greatly accelerated due to Covid-19 as the need for contactless processes … Read more
eRegulatory Binder Checklist: What Does the FDA Require?
eRegulatory binders help clinical sites organize and digitize the regulatory process, but each binder is different depending on the specific clinical trial site protocol. Here, we provide an overview of the specific sections and documents that must be included for an FDA-regulated study.