eCRF Software for Clinical Trials
Solution Everything you need to configure, manage, and leverage your clinical research trials, from data collection to final analysis.
Design and Deploy Your Clinical Trials
Our eCRF software adapts to your protocols, allowing you to customize forms and workflows in minutes with no coding required. Test your study in real time and launch it quickly with compliant data collection.
Collect and Validate Your Clinical Data
Collect clinical data through structured eCRFs tailored to your protocol. Edit checks, validation rules, and query management help you quickly identify missing or inconsistent data and improve data quality.
Monitor Data Collection in Real Time
Track data collection from a centralized dashboard, including enrollment progress, eCRF completion, missing data, and queries. Quickly identify areas requiring attention.
A Comprehensive eCRF software
Solution Everything you need to configure, manage, and leverage your clinical research trials, from data collection to final analysis.
Sample size
Calculate the number of subjects to include in your study in seconds.
Customization
A code-free, fully configurable eCRF that adapts quickly to your protocols and study designs.
Import
Monitoring
Manage queries to flag and correct missing or inconsistent data, keeping your study data accurate and audit-ready.
Audit Trail
Export
Customer success story
“An intuitive eCRF that we can configure ourselves. One of our diabetologists was delighted to be able to analyze everything for himself!”
Caroline Allix-Béguec
Head of clinical trial department
EasyMedStat adapts to your needs
Choose only the modules you need. Combine them to build a powerful and scalable clinical data software.
Create your eCRF in minutes using a no-code interface. Our clinical EDC meets the highest standards for electronic data capture in clinical research and clinical trials.
eCRF
ePRO
Gather patient-reported information with ease. Create and implement unique surveys that are completely integrated into your EDC and offer flexible ePRO scheduling.
Data monitoring
Centralize data review and monitoring activities.
Open, assign, and resolve queries from a single dashboard to ensure high-quality, reliable clinical data.
Guided Statistical Analysis
The only EDC with native statistical tools. Analyze your data with an integrated sample size calculator, Student’s test calculator, chi-squared tests, and an intelligent data cleaner, no technical expertise required.
Frequently asked questions
Do I need advanced statistical knowledge to use EasyMedStat?
Not at all. The platform offers guided workflows and automated analyses tailored to the most common needs in clinical research. You can run robust analyses without having to master complex statistical methods.
How does EasyMedStat handle data traceability?
Every action taken on the platform is automatically logged: data edits, analyses, and exports alike.
Each event is timestamped and tied to an identified user, giving you a complete, reliable audit trail at all times. That trail covers the full history of every project, so you can track every data manipulation step with total transparency and walk into any audit or inspection fully prepared. And because the system is designed to meet the requirements of clinical research environments, you can count on full action history retention and data integrity throughout the entire project lifecycle.
Is EasyMedStat built to grow with my research?
Yes and on every front.
The platform scales across project types, from straightforward studies to complex protocols, with modules that can be configured to fit your specific needs. EasyMedStat is regularly updated with new features and performance improvements to keep pace with evolving clinical research practices. And whether you're managing a small dataset or a large, multi-site database, the architecture is built to handle growing data volumes without any drop in performance.
GDPR Compliant Platform
EasyMedStat meets all applicable standards and requirements for both interventional and observational clinical trials: ISO 14155, Good Clinical Practices (GCP), MDR / EU MDR, and GDPR data protection obligations. Data is hosted on an HDS-certified infrastructure, ensuring the highest level of security required by pharma and biotech companies. This built-in compliance reduces regulatory risk and simplifies audits and inspections.
How much does it cost?
EasyMedStat is based on a flexible, modular pricing model designed to adapt to the needs and budgets of medical device manufacturers, whether startups, SMEs, or large groups. You only pay for the modules you actually need (eCRF, ePRO, monitoring, statistics, etc.), reducing costs compared to heavier solutions or full outsourcing.
The goal: a comprehensive, accessible solution tailored to the regulatory requirements for your clinical studies
