Automated Statistics

Built for clinical research, designed for speed

Run Statistical Analyses On Your Own

A no-code statistical environment built for clinical and research teams , so you can produce reliable analyses without relying on external providers.

Leverage Your Existing Data

Easily use existing databases, retrospective studies, registries, or real-world data (RWD),  to produce exploratory analyses, reports, or scientific communications

Turn Investigator-Initiated Trials Into Published Research

A simple and comprehensive environment to support IIT studies from start to finish, deliver reliable, clean, and reproducible results, and share actionable analyses in a single click

A Full Statistical Toolkit

Built for clinical research, designed for speed
Data cleaning

Use the Data Cleaner to flag inconsistencies, outliers, and completeness gaps, ensuring data quality and centralized monitoring throughout your study.

Automated test selection

The tool automatically selects the most appropriate statistical test based on your data and clinical question, in line with clinical research standards (Fisher's test, Chi-squared test, Student's t-test, etc.).

 Univariate and multivariate analyses
Run univariate and multivariate analyses, including logistic regression, to quickly surface predictive factors in your biostatistics workflow.


Survival analysis

Run survival analyses using the Kaplan-Meier estimator to compare patient groups and visualize survival curves.

Publication-ready outputs
Auto-generate structured statistical write-ups for the Methods and Results sections of your manuscript , reducing misinterpretation and cutting back on reviewer comments.

Export
Download datasets and results in standard formats for seamless integration into reports, abstracts, and journal submissions.

Customer success story

"EasyMedStat supports our long-term studies, as the integrated statistical tool allows our project managers to quickly generate PMCF reports.”

Cedric Ferry

Class III Clinical Project Manager 


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
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patient visit inclusion survey
ePRO
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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
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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
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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