About Devana Solutions®:
A Company on a Mission to Reduce the Cost of Healthcare and Cure Disease through Technology
We connect the best Research Sites with Sponsors and CROs to reduce drug development costs and cure disease.
Devana Solutions®, LLC is a SaaS provider driven by a core belief that data transparency through technology is critical to selection of the top performing research sites to align with pharmaceutical Sponsors and CROs to reduce drug development costs and cure disease. Devana Solutions® offers three platforms, IGNITE for sites, PROPEL for networks and IQ for Sponsors and CROs, to provide historical and real-time data capture, aggregation and display to drug development stakeholders.
At Devana Solutions®, our unwavering commitment to this core belief inspires the cloud-based technology platforms we build, license and support.
Drug Sponsors & CROs must find and select the best research sites – those that consistently recruit, screen and enroll more patients, faster and safely while gathering clean, accurate data on a drug’s safety and effectiveness – to REDUCE CLINICAL TRIAL CYCLE TIME and drug development costs.
IQ for Sponsors-CROs reduces site selection risk for Sponsors and CROs by providing full transparency into an investigative site or site network’s historic and real-time performance and timing metrics data, improving trial feasibility and performance while reducing clinical trial cycle time and costs.
IGNITE for sites arms investigators, research sites and site networks with time-saving automation and powerful data to reduce study start-up, improve operations and win more study awards in less time. Use the technology to prove your therapeutic strengths, enrollment capabilities and operational-expertise by easily reporting and displaying timing and performance metrics to CROs and Sponsors.
Gain total transparency into your site or site network’s historic and real-time performance – both good and bad – and use these analytics to help your management team improve study operations and performance and therapeutically and operationally align with the right Sponsors and CROs.
Save valuable time for your site managers by centralizing and automating your contacts, pipeline and document administration to track study leads and capture critical timing and performance metrics datapoints all the way through trial completion and close out.