Choose the plan that fits your needs
Registry, Single Study, or Unlimited Studies. Secure, scalable, and GDPR-compliant solutions
Registry
Unlimited users
1 active registry
Pick the modules you need
Premium support
Single Study
Unlimited users
1 active study
Pick the modules you need
Secure hosting + premium support
Multiple Studies Plan
Multiple studies
Pick the modules you need
Secure hosting
Premium support
More than 200 companies of all sizes trust EsymedStat.
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.
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 reviewed journals
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
