Electronic Data Capture Designed For Your Needs

Streamline and simplify your clinical data management with a flexible suite of tools.

Compared to other EDC solutions on the market from MediData, DataTrack, Omnicomm and others, TrialStat is the most all-encompassing suite of study management tools that can be seamlessly connected to external data sources such as EMR, wearables, and other clinical and non-clinical data and information sources.

TrialStat offers a fully unified platform suitable for all phases and types of trials. Our single-sign-on, multi-tenant EDC suite includes modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, Vendor Neutral Imaging Archive, a robust Reporting and Analytics Portal and custom Machine Learning programs.

With a focus on data analytics, TrialStat offers real-time reporting, data extracts on demand, and analytics across a single study, a program, or your entire research portfolio – providing all stakeholders relevant, customized, timely insight into all aspects of study data and highlighting areas of risk or potential delays.

Explore Our Advanced Modules & Capabilities

Randomization / IWRS

TrialStat EDC provides integrated IWRS functionality, allowing for any degree of randomization complexity.

Using TrialStat IWRS will enable sites to trigger randomization codes directly without leaving TrialStat EDC, and without the need or added cost of another software system.

Our user-friendly system implements the most current technologies and tools to ensure that your team can successfully randomize patients into your trial without complications or delays.

Click the diagram below to explore all of the features of the TrialStat eClinical Suite.

ePRO
Medical Coding
Vendor Neutral Imaging Archive
Adjudication
Clinical Data Warehouse
Machine Learning Programs
3rd Party Systems Integration
Study Design and Validated Development

Request Your Demo Today!

From rapid database build through database lock, we deliver consistent quality on-time and on-budget. Ready to upgrade your eClinical toolkit?

A Fully Unified eClinical Suite with Premium Features and Capabilities

Solution of choice for the successful execution of over 500 clinical trials.

Of those trials, 96% of studies launched on time and database lock happened within 10 days on more than 92% studies.

Built to meet the needs of users across all study phases including pilot / proof of concept studies, Phase I, II, III and IV studies, as well as medical device and diagnostics.

Access from any browser, mobile device, tablet, laptop or desktop computer, without the requirements of any proprietary browser plugins or desktop software installs.

A Fully Unified eClinical Suite with Premium Features and Capabilities

eSource

Completely Customizable eCRFs

CDASH Compliant CRF Library

Randomization / IWRS

Inventory Management

CDASH Compliant CRF LIbrary

Integrate Real World Data

Patient Reported Outcomes (ePRO)

Browser Based & Mobile Responsive

CTMS

Comprehensive Edit Checks

Dynamic Skip Logic & Comprehensive Edit Checks

HTML 5 Complicant DICOM Viewer - CE Class IIa Certified

Image Management

2-4 Week Build Time

Configurable Study Workflow

Real-Time Data Visualization

Make Critical Decisions Sooner

Flexible Data Capture

Bar Code Integration

Real-Time Monitoring, Reporting & Validation

Integrated Real-Time Reporting

Multi-Lingual Support

Replicate Entire Studies

40+ Standard Reports

Configurable Reports & Dashboards

Drill Down Into Your Data With Interactive Reports

See TrialStat In Action

Request Your Personalized Demo. Our Clinical Team will organize a tailored demonstration of TrialStat based on your specific study requirements.  You'll see first hand how TrialStats unified features, blazing speed, configurable features and comprehensive functionality will help you run more efficient and cost effective studies.