Product Overview
Stay on top of your trial with real-time access to study documentation using the EvidentIQ eTMF. Easy to use and easy to manage. Create your own workflows to route documents – eliminating tedious manual processes. eTMF filing is embedded within our CTMS to streamline processes.
Provides a quick oversight into the quality, completeness and timeliness of your trial documentation. Use our dashboards or create your own to display study health and to monitor inspection readiness. Use EvidentIQ’s eTMF as a stand-alone eTMF or inherently integrated with the rest of our platform – providing a single sign-on for all your clinical trial software needs.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Flexible File Structure keeps you in control
You have complete control over the folder new person, new monitoring visit) structure, what documents you want to collect and what metadata you want to collect about them. Start from scratch or begin with our out-of-the box DIA reference model configuration (included at no
additional cost).
Intelligent Placeholders
Document Sets are created automatically based on events that occur (e.g. new site, You have complete control over the folder new person, new monitoring visit).
Integrated eISF
Provide your sites with access to the integrated eISF, reducing burden for your sites and your monitors while ensuring oversight of clinical trial documentation.
Cost Effective
Subscription based software with no per study fees. Use in conjunction with our CTMS for even more cost efficiencies
About the company
Leveraging more than 50 years of combined experience providing innovative and creative ways to conduct clinical trials. End-to-end eClinical Solution
Meeting increasing customer demand across clinical operations and clinical data management needs with a suite of applications within a single integrated cloud platform, including EDC, CTMS, eTMF, eCOA, coding, remote monitoring, RBM, RTSM, Payments and eFeasibility. Geographical Reach
In-country patient communities platform in North America and Western Europe (EU5) and ability to conduct studies at a broader scale (LatAM, Asia…). Regulatory expertise to support broader geographical studies.