Modern Electronic Data Capture Solution (EDC)

Solution Everything you need to configure, manage, and leverage your clinical research studies, from data collection to final analysis.

Design and Deploy Your Clinical Studies

Our EDC solution fits your protocols, customize forms and workflows in minutes, no coding needed. Run real-time tests and launch your study quickly with clean, compliant data

One Platform for All Your Clinical Data

Bring together EHR, eCRF, ePRO/eCOA, and API data in one place to eliminate re-entry, sharpen analysis accuracy, and move from data collection to insights faster.

Stay on Top of Your Studies with Full Visibility

A centralized dashboard to track progress, key milestones, and data integrity across the entire study lifecycle, in real time.

A Comprehensive EDC/eCRF

Solution Everything you need to configure, manage, and leverage your clinical research studies, 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
Bring in an existing dataset or build your study from the ground up, your choice.


Monitoring

Manage queries to flag and correct missing or inconsistent data, keeping your study data accurate and audit-ready.

Audit Trail
A complete, timestamped log of all actions and edits, ensuring full data transparency and integrity throughout the study.

Export
Pull your data at any time in formats ready for import into standard analysis tools, making sharing and archiving seamless.

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
""
patient visit inclusion survey
ePRO
""

Gather patient-reported information with ease. Create and implement unique surveys that are completely integrated into your EDC and offer flexible ePRO scheduling.

Patient questionnaire screen asking how the patient is feeling today
Data monitoring
""

Centralize data review and monitoring activities.
Open, assign, and resolve queries from a single dashboard to ensure high-quality, reliable clinical data.

EasyMedStat Query Lifecycle
Automated 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