The Single Interface®
The Single Interface® gives you single-access to all your data
The Single Interface® gives you single-access to all your data
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.
On-tap Analytics, Dashboards and Visualizations on everything, including Visual Patient Profile and ad-hoc report building.
Collect data at the sources and manage queries, CRF locking and transfers
Track monitoring activities and manage data cleaning, SDV and report activities
Collect, approve, organize and process essential documents
Randomize patients, dispense study drug and track investigational product distribution, reconciliation & destruction
Receive, process and generate reports for safety events with auto-populated MedWatch or CIOMs forms
Automate investigator grant invoicing, reconciliation, payment and reporting
Obtain real-time, real-world patient efficacy and safety data to improve quality and compliance
Improve accuracy and consistency of clinical endpoint adjudication data and streamline CEC review
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.
Ready to see how Prevail’s Single Interface® can help you improve
clinical development and achieve better outcomes?
