Powerful, efficient, and easy to use study management solutions
The right clinical trial management system is your coordination hub, logging and tracking all the moving pieces of your study and ensuring that your team has real-time visibility into issues, study progress, and potential areas of risk.
TrialStat CTMS provides the robust functionality needed to manage the most complex studies with the ease of use that busy teams require.
Enables oversight of related clinical trials per therapeutic area based on a set of specific clinical project activities (i.e., tracking actual vs. target). Includes the ability to track progress at specific trial and program levels.
Facilitates investigator and site identification and recruitment, including key trial milestone tracking such as target site/enrollment metrics for each study country.
Provides tracking ability for site monitoring, subject enrollment relative to plan, and Case Report Form (CRF)/ Electronic Case Report Form (eCRF) completion status. Includes management of site visits/trip reports.
Tracks key information such as CRF collection, Clinical Research Associate (CRA) monitoring frequency, protocol visit frequency, and adherence to protocol regiments. Includes support for study documentation and tracking tasks.
Supports financial management including tracking study costs, reimbursing investigators, and paying claims related to study activities. Includes grant payment management and management of financial disclosure.
Clinical supply management including supply tracking.
Provides reporting/dashboards to communicate trial performance against targets, as well as other operational reports.
Ability to connect TrialStat CTMS to existing technology solutions for seamless data exchange and reporting.
TrialStat CTMS Screen Shots
A Fully Unified eClinical Suite with the following Premium Features and Capabilities
"TrialStat CTMS is flexible, affordable, and easy to use. Our studies run more smoothly now, and we have the data we need when we need it in order to make key decisions or address issues. The support team is fantastic too!"
— Study Manager, Start-Up Biotech, West Coast US Region
"We appreciate the ability to view our current data with TrialStat's customizable reports. Along with the standard metrics reports for management oversight, this feature allows us to view unlimited combinations of data in real-time."
— Manager, Clinical Operations, Device Sponsor, Mid West US Region
"We contracted with TrialStat to handle the Electronic Data Capture for two large-scale clinical endpoint bioequivalence trials conducted in the US and globally. We have been extremely happy with their performance. In our last study, database lock occurred approximately 24 hours after the last patient completed the trial!"
— Director, Clinical Development, Major US Client in Northeast US
See TrialStat In Action
Request Your Personalized Demo. Our Clinical Team will organize a tailored demonstration of TrialStat EDC, TrialStat Portal and TrialStat CTMS based on your specific study requirements. You'll see first hand how the TrialStat unified features, blazing speed, configurable features and comprehensive functionality will help you run more efficient and cost effective studies.