Driving Study Site Performance
TriPort is a multifunctional investigator portal spanning training, documents, communications, safety reports, dynamic FAQs, patient visit guides, site engagement and other capabilities.
TriPort improves study quality and efficiency in a format that is easy to access and simple to use. With one sign-on, study managers, CRAs and investigator sites gain access to an array of function-rich centers that can be selectively activated to fit the needs of each clinical trial.
Study managers and CRAs benefit from custom views that keep them better informed, and tools that vastly improve their ability to complete key tasks. Investigative sites benefit from functions that make it clearer to organize and easier to complete core activities, with improved speed and quality.
More than an Investigator Portal, TriPort is an Ecosystem of Study Solutions.
Single
Sign-on
Personalized access to TriPort, Study eSafe, InSite Virtual Monitoring and Stratus Advisory Portal.
Training
Deliver effective role-based training with consolidated records and site-level views.
Documents
Easily assign, distribute and view real-time status of document completion.
Safety Reports
Streamline the safety reports process with better workflows and real-time tracking.
FAQs
Easily manage role-based FAQs, giving sponsors, CRAs and sites the answers they need.
Correspondence
Improved speed, convenience, and security of messaging, with superior workflows.
Protocol
Mobile access to a more searchable and informative Study Protocol.
Dashboard
A personalized gateway to the platform, simplifying completion of items requiring attention.
Metrics
Simplified access to visual metrics on key activities, with drill-downs and reports.
Tracking
Convert insights into action with tools to drive high rates of site task completion.
Monitoring
Empower CRAs with superior technology for remote management of site monitoring.
Engagement
Drive site engagement with leaderboards, news, site awards, discussions, surveys and more.
Visit Guides
Mobile access to a check list of procedures for each visit, with protocol hot links.
Visit Calculator
Calculate accurate dates for each patient visit, with reminders and a central calendar.
Related Resources
Strategies to Optimize Study Site Training Effectiveness
Avoid the Front-loaded Training Paradigm During the go-live period in a clinical trial, study teams and CRAs are under…
Relieve your CRAs of the Site Training Burden
CRAs are tasked with an ever-increasing number of tasks and responsibilities to ensure that trials are running smoothly. One…
Revolutionizing Drug Safety Report Distribution with TriPort Trial Portal: A Seamless Approach
In the fast-paced world of clinical trials, effective drug safety reporting is paramount. However, navigating the complex…