The data you need.
The precision to make it count.
Accelerating clinical trials through the power of connectivity & data
Never has the clinical trials industry been so critical. That’s why leading clinical research organizations turn to Devana Solutions for our bleeding-edge cloud-based products and services.
Fortifying collaboration between on-site and decentralizied research teams as well as clinicians serving patients in diverse communities is the foundation of our innovative, real-time, value-focused platform.
What Our Solutions Can Do For You
29.7 hrs
saved per week
40%
increased revenue
58.6%
ROI
14.25 hrs
saved per study activation
76%
reduced contract and budget turnaround time
29.7 hours - Analysis by leading IRO (Integrated Research Organization) based on 100 new trial activations per year
40% increased revenue – By leading global site network client, 2020 vs. 2018
58.6% ROI – Estimated time savings during trial startup, activation plus increased productivity, leading IRO, approx. 100 trial activations per year
14 ¼ hours – same footnote reference as 58.6% ROI above
76% - Global Site Network, analysis conducted 6-months post-Devana PROPEL implementation vs. basic CRM combined with spreadsheets to track startup milestones
Better data.
Better decisions.
Better outcomes.
For sites, site networks,
sponsors, and CROs
FOR CLINICAL OPERATIONS TEAMS
Seamlessly share crucial data across your clinical research organization. Enable connectivity and collaboration between your centralized team and decentralized staff and study teams at Site Networks, IROs, SMOs, CROs, AMCs and Health Systems.
Instantly Aggregate Data
“The CRO couldn’t believe it! Within seconds of my introduction, they were holding reports and dashboards validating the predictability and reliability of our sites in the indication!”
Jeff Kingsley | Chair, COO & Founding Member | hyperCORE International
Recent News
Advancing Clinical Trial Site Management: Strategies for Improved Performance
One common frustration in the initiation phase of clinical trials is the frequent occurrence of delays. In an analysis published by Nature, nearly a quarter of all trials experienced setbacks due to strategic issues, commercial barriers, and operational … Read More
Transitioning from Paper to Electronic Workflows in Clinical Trials with PROPEL
Clinical trials play a pivotal role in advancing medical research and bringing new treatments to patients. Traditionally, trials have been conducted using paper-based methods for startup activities and beyond, such as negotiating Confidentiality Disclosure Agreements (CDAs) and managing … Read More
Why Your Clinical Research Site Needs More Than a CTMS
Clinical trials require precise management across various domains such as patient recruitment, data collection, regulatory compliance, and stakeholder communication. While Clinical Trial Management Systems (CTMS) have been pivotal in organizing and simplifying many of these aspects for clinical … Read More