5 Crucial Considerations for Selecting a CTMS

scientists-working-on-research-in-lab

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

RealTime Mobile App

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

Bringing 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

Take Clinical Trial Management to the Next Level with LYNK

LYNK upgrades your sites’ clinical trial management capabilities by allowing them to manage trial opportunities and quickly and easily complete feasibility assessments.

As a technology provider that connects central trial operations teams with decentralized site staff and clinicians, our goal at Devana Solutions is to help research organizations speed new therapies to patients by automating clinical trial processes and capturing site metrics for analysis and execution. You may be familiar with PROPEL, our enterprise-level platform for managing … Read more

New Customer Feature Request Form Brings Ideas to Life

Need a new feature or solution in the RealTime system?

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

IMA Clinical Research Adds Devana Solutions’ PROPEL Clinical Trial Data Platform

IMA Clinical Research Adds Devana Solutions' PROPEL Clinical Trial Data Platform

Bringing the Clinical Trial Site to the Patient: IMA Clinical Research Adds Devana Solutions’ PROPEL Clinical Trial Data Platform   While 2021 certainly had its ups and downs, the Devana Solutions team is delighted to say we were able to end the year with a BANG! This past year we focused on accelerating clinical trials … Read more

Data Analytics & Making Decisions for Better Outcomes

data analytics, clinical trial industry

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

Learn More About Devana Solutions Clinical Trial Data Platform

How Technology Simplifies Clinical Trial Feasibility Assessments Ah, the dreaded site assessment and feasibility: pages upon pages of requests for information. From equipment specifications to investigator experience to patient population, the amount of data needed to execute a clinical trial feasibility is onerous. You may have most of this information on hand—across a variety of … Read more

Pros and Cons of e-Signatures in Clinical Research

Pros and Cons of eSignatures in Clinical Research with CEO Rick GreenField Blog

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?

eReg Binder

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.