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eCRF at the Service of Your Clinical Studies

EOL© is the data-collection and management solution for your observational studies and registries
A simple, robust, cost-effective SaaS model

More than just an eCRF provider
We support you from design through delivery of your eCRF

Design your own studies with EOL Conception©
the most comprehensive study-designer on the market

Data security in France within an HDS-certified (Health Data Host) environment

Agile and responsive
Deploy your eCRF in just a few weeks

User-centric, EOL© is built to simplify the work of investigators, monitors, data managers, and project managers

EOL© the intuitive solution that's easy for investigators to learn and use

EOL© is the application designed for investigators, Arc monitors, data managers and clinical trial project managers

EOL© is the data-collection and management solution for your observational studies and registries
A simple, robust, cost-effective SaaS model

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Our EOL Suite Modules

eCRF

EOL© is more than a simple data-entry tool, it’s a full application built specifically for clinical research...

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EOL Conception©

The market’s most comprehensive study designer, letting you build your own eCRFs and ePROs, program reminders, and more...

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ePRO

Improves subject experience and cuts study costs with direct patient questionnaires on mobile or web...

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eConsent

Enables investigators to send electronic consent requests via the eCRF before enrolling patients...

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EOL Random©

An IWRS for your randomized trials, integrated in the eCRF or used externally...

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EOL Pharma©

Treatment-unit management module for dispensing and stock replenishment, with or without randomization...

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EOL©, the 100% Web-Based eCRF

All modules, from design to randomization, monitoring, data management, and administration, are accessible online.

Advantages for your studies :

Shared maintenance and hosting costs,
24/7 data availability,
Confidentiality and security tailored to healthcare requirements,
Fast and simple deployment,
Agility to create/manage sites and investigators during the study,
Agility to create/manage sites and investigators during the study,
Full autonomy for your teams throughout the study.

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EOL© in a Few Figures

25+

years of experience

observational
registries

102

nterventional
studies

230

non-interventional studies

They Trust Us

AFCP – French Association of Foot Surgery

We needed a reliable, cost-effective solution accessible across France. Medsharing’s responsiveness, adaptability, and the software’s usability—virtually training-free—have fully satisfied us. We use the EOL software directly in the operating room.

Read the AFCP Success Story

RENAPE – National Network for Peritoneal Rare Tumor Care

Thanks to Medsharing’s responsiveness and intuitive, fully SaaS, configurable software, over five years we enrolled more than 1,500 patients. It empowered sites, improved data quality, and set the stage for registry sustainability and international expansion.

Read the RENAPE Success Story

Client References

A Certified, 100% Secure Environment

At MEDSHARING, data quality and security are at the heart of our commitment. Our cutting-edge digital tools comply with all regulatory requirements, ensuring reliable and secure clinical-trial management.

Our certified, internationally-recognized expertise :

ISO 9001 (registration No. A00820) for all management and engineering processes,
FDA 21 CFR Part 11 compliance for data security and electronic signatures,
EU directive 2001/20/EC and French law of August 9, 2004 compliance for clinical-trial standards,
GDPR-compliant protection of sensitive personal data.

A highly secure infrastructure

All studies are hosted on a centralized, independent, HDS-certified platform in France via our partnership with OVH, ensuring secure storage that meets the strictest medical-sector requirements.

With MEDSHARING, choose a reliable, compliant, and secure solution to conduct your clinical studies with confidence.