Collect, structure, and leverage your clinical research data. A complete and intuitive clinical data platform designed to accelerate EDC in clinical trials, data analysis, and scientific publications.
Choose only the modules you need. Combine them to build a powerful and scalable clinical data software.
Create your EDC/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.
EDC/eCRF
eCOA/ePRO
Gather patient-reported information with ease. Create and implement unique surveys that are completely integrated into your EDC and offer flexible eCOA 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.
Real impact on your clinical studies
Discover how EasyMedStat simplifies study execution, secures your data, and significantly reduces analysis timelines.
Fast and intuitive onboarding
Thanks to a no-code, intuitive interface, your teams become autonomous quickly even without technical or data management expertise.
Designed in accordance with ISO 14155, Good Clinical Practice, and European regulatory frameworks, EasyMedStat provides a secure, traceable environment ready for audits, inspections, and submissions.
Investigators, CRAs, biostatisticians, data managers, and quality teams collaborate on one platform with role-based access and centralized communication.
Every action is recorded in a secure, time-stamped audit trail compliant with regulatory requirements, ensuring data integrity and simplifying inspections.
A flexible EDC for mono- and multicenter studies and registries, designed to streamline data collection and optimize research workflows.
CROs
Deploy studies faster, manage more trials in parallel, and reduce data management workload for your sponsors.
Medical Device Manufacturers
A flexible eCRF platform compliant with international regulations, designed for pre-market and PMCF medical device studies, ensuring data integrity and traceability.
Pharma & Biotech
EasyMedStat helps pharma and biotech clinical trials teams support investigator-initiated studies with a ready-to-use EDC designed for KOLs.
Learned Societies
A flexible EDC platform designed for learned societies, built to manage registries, multicenter studies, and real-world data collection
4 weeks
Required in average to start your study
2 x faster
Cut the time you spend on statistics in half
350+ articles
Have quoted EasyMedStat in peer-review journals
They run their studies with EasyMedStat
Here’s what our users say about their experience.
“An intuitive EDC 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 is part of our strategy. As part of our promotional activity, we needed an intuitive tool that met our expectations.”
Stéphanie Durel-Pinson
Head of clinical research - Vivalto Santé
“The responsiveness and professionalism of EasyMedStat confirmed our choice of solution.”
Delphine Agullo
PDG
eCRF / Clinical EDC
Create your eCRF in minutes using a no-code interface.
