The Single Interface® provides a complete and real-time picture of your studies. All of your clinical, diagnostic, operational, logistical, and accounting data is automatically and continually integrated from any source into a central repository, quality controlled, and leveraged with advanced analytics, visualizations, and workflow tools for early observations, optimal decision and process support, and seamless vendor coordination.
The Single Interface® is also your single sign-on for all Prevail clinical trial systems, including EDC, eConsent, eTMF, Safety System, ePRO/eCOA, Grant Navigator for Investigator Payments, RTSM etc.
The normal implementation period of the Single Interface® is 4-7 weeks, which is done by Prevail under a software-as-a-service model, including all data integrations, visualizations, and reporting engines.
Automate labor-intensive manual tasks to proactively manage key deliverables and enable predictive modeling so you are always one step.
Aggregated data is normalized, reconciled and reported with as much automation as possible, including triggered alerts and other role-based messaging.
The Single Interface® provides early observations of aggregated data for reconciliation, taking advantage of tools and systems integrations to support holistic views and timely role-based reporting.
We are so confident in the value we provide that we offer a 100% no-questions-asked money back guarantee.
Developing software to solve major challenges unique to clinical trials, leading to important innovations reflected in 17 US patents (296 claims) with broad applicability.
20+ years of clinical operations experience, from Phase I to Phase IV, in hundreds of trials in every major therapeutic area. Personnel with decades of clinical trial and engineering know how.
Our systems are validated and delivered according to US and International regulations, such as 21 CRF Part 11/Annex 11 and ICH GCPs.