Devana Solutions IGNITE is an easy-to-use software platform that simplifies the complex pipeline management process by consolidating all trial opportunities in one place. IGNITE makes the management of business development, contact management, start-up activities, study execution and performance metrics easier and faster. Further, IGNITE has integration capabilities with key CTMS systems for end-to-end operational excellence.
- Pre-CTMS data collection, aggregation and analysis for quick decisioning
- Data transparency and mobilization across all stakeholders – standard reporting
- Real time trial pipeline view and tracking of key contacts, documents and tasks
- Automated task follow-ups and reduced emails outside of system
- Ability to link multiple contacts, documents and correspondence to every study opportunity
- Cloud based, data security
Automate Start-up, Analytics and Reporting across Your Network
Our innovative network platform extends the IGNITE technology and incorporates advanced capability to seamlessly manage your expansive network of owned and affiliate research sites, up to several hundred locations. Automate your contacts, pipeline management and operations across your network. Our PROPEL platform allows you to localize trials to the most effective sites across your footprint – saving time and costs in study start-up while building your network’s reputation for reliable performance. In just a few clicks, aggregate and analyze data, in real time, to improve trial performance. Finally, display your metrics data in clear reports that allows your leadership to be current on performance and enable better decision making that aligns with Sponsors and CROs requirements.
With IQ, Sponsors and CROs have access to historic and real-time site performance data to identify, select and align with the best research site operators.
With Devana Solutions IQ for sponsors-cros, top research sites, site networks and academic research centers, using Devana’s companion data analytics technology, can share historic and active trial performance data leading to true operational-alignment with Sponsors/CROs.
Sponsors and CROs can view and evaluate tangible, reliable data from partner-sites. No more dependence on sites’ self-prepared, hard-to-verify feasibility submissions. Sponsors and CROs can view and evaluate tangible, reliable site performance data vs. traditional, hard-to-verify feasibility submissions. This data transparency reduces site selection risk and improves feasibility through more predictable performance.
Sponsors and CROs aligned with top investigative sites through performance data transparency will complete clinical trials faster and for less costs speeding new therapies to patients.