The company was founded at the initiative of an investigator–surgeon specializing in clinical research.
Since then, MEDSHARING has been designing and marketing web applications dedicated to clinical research for more than 20 years.
Our Growth
Very quickly, we focused on eCRF by developing a comprehensive data-capture solution: EOL© (Étude On Line), which integrates monitoring, validation workflows, data export, and randomization.
Since 2006, we have held ISO 9001 certification for all our management and engineering processes.
We comply with FDA 21 CFR Part 11 and adhere to French and European regulations on health-data management, notably Good Clinical Practice (Directive 2001/20/EC of April 4, 2001 and the August 9, 2004 law) and the GDPR.
Over the years, our offering has expanded into several standalone services, including :
- EOL Random© (Internet-based randomization),
- EOL Consent© (electronic consent),
- EOL Pharma© (treatment-unit management).
A Solution for Every Type of Study :
- Therapeutic trials, clinical studies, randomization,
- Pharmaco-epidemiological studies,
- Material-or pharmaco-vigilance,
- Registries, observatories, cohorts,
- Nutraceutical (“alicament”) studies,
- Medical-marketing surveys.
EOL© serves all research stakeholders, both public and private.
Institutional Actors :
- INSERM and CNRS units,
- Research agencies,
- Public-health monitoring institutes,
- Academic associations and consortia,
- Regional Clinical Research Departments (DRRC).
Private Actors :
- Contract Research Organizations (CROs),
- Pharmaceutical industry,
- Medical-device industry,
- Food-industry,
- Cosmetics and para-pharmaceutical industry.
