Easily Migrate from edc2go!

Trust TrialStat to Migrate Your Study from edc2go!

Don't be held hostage by your CRO or EDC Vendor. Take ownership of your study data and benefit from a Fully Unified eClinical Suite.

With the discontinuation of edc2go, now is the time to rethink which Electronic Data Capture Vendor and Platform to trust your current and future studies with.

Established in 2003 and backed by Jubilant Life Sciences, TrialStat has completed over 500 Clinical and Device studies around the world.

Our team of clinical professionals have invested extensive resources, combined with feedback from users like you, to develop and expand our robust, flexible, and easy-to-use trial management suite, making it easier for you to manage and report on all facets of your study.

With robust, integrated tools such as IWRS, ePRO, Coding, CTMS, and reporting Portal, TrialStat's suite of study management tools are an ideal fit for busy study managers and clinical operations professionals looking to resource a cost-effective solution that will elminate challenges and simplify their vendor roster.

Rescue Studies, Data Migration & New Studies

Whether you have current studies on edc2go or new studies starting, trust TrialStat's team of Professional Project Managers to safely migrate those studies and configure and launch your new ones.

At the same time you can use this opportunity to resolve all of your outstanding study challenges and take advantage of the additional time and cost saving features TrialSTat has to offer.

Stop The Uncertainty And Partner With a Vendor That Will Take Care of You And Your Studies!

Give us a call today and speak with our Clinical Team to discuss how we can help you solve your current challenges and let you focus on what matters most - running your studies!

Reach us by phone (1-888-488-0312), email ([email protected]), or submit this form to request your personalized demonstration of TrialStat today.

Why Migrate To TrialStat?

Experts in Rescue Studies and Study Migration

Comprehensive Unified Platform

New Features Released Regularly

Resolve Outstanding Study Issues

Superior Customer Service

Benefit From Happier and More Efficient Sites

Work With Fewer Vendors

Real-Time Visibility across all your studies

Reduce Overall Study Risk

Address and Phone

16751 Trans Canada Highway
Kirkland, Quebec
H9H 4J4, Canada

Telephone: 1-888-488-0312
Fax: 613-274-3674

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.

A Unified eClinical Suite Delivering Real-Time Data

eConsent Module

Randomization Module

ePro (Patient Reported Outcomes) Module

Medical Coding Module

IWRS & Inventory Management

Vendor Neutral Imaging Archive (VNA)

Browser Based & Mobile Responsive

CTMS by SimpleTrials

Comprehensive Edit Checks

Dynamic Skip Logic

AE / SAE tracking

Fully Customizable eCRFs

Fully Customizable Data Review Status Work Flows

DICOM Image Viewer(s)

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

Data Drill-Downs

Regulatory Compliance

TrialStat's entire Unified eClinical Suite is developed and deployed with an Agile Methodology and specifically engineered to comply with FDA 21 CFR Part 11 requirements for Electronic Records and Electronic Signatures, HIPAA, GDPR and FISMA. TrialStat maintains a Master Validation Plan and Change Control procedures.

GDPR and HIPAA Compliant

21 CFR Part 11

Good Documentation Practices

Privacy Shield

Electronic Signatures

Change Control Procedures

Full Audit Trail

SAS 70 Type II

CAPA Program

SOX Compliant Solutions

FISMA Compliance Solutions

Quality Management System