MEDSHARING designs and provides EDC and eCRF solutions over the internet in medical expertise and clinical research for over 20 years.

We quickly specialised in e-CRF by creating a global solution to collect EOL© data (OnLine Study) with monitoring, validation system and data export.

Since 2006, we have been certified ISO 9001 version 2008 for all of our management and engineering processes. We are compliant to FDA 21 CFR part 11 and HDS hosting. We meet the French and European regulations relations to health data (Directive 2001/20/EC of April 4, 2001 and the Act of August 9, 2004).

Over the years, our range has grown and provides different services that can be used independently such as EolRandom© (randomisation via internet), eConsent (electronic medical consent), eProduct (Study drug management ), ePro (electronic patient reported outcom)


EOL© is suitable for all types of medical and para-medical studies:

- Therapeutic tests, clinical studies, randomisation
- Pharmacoepidemiological studies
- Medical device or pharmaco-vigilance
- Records, Observatories, Cohort Studies
- Studies on functional foods
- Medical-Marketing surveys

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