MEDSHARING designs and provides EDC and reporting solutions over the internet in medical expertise and clinical research for over 15 years.
The company was founded by a surgeon investigator, who was a specialist in clinical research.
We quickly specialised in eCRF by creating EOL© a global solution to collect data (OnLine Study) with monitoring, validation system and data export.
Since 2006, we have been certified ISO 9001 for all of our management and engineering processes. We are compliant to FDA 21 CFR part 11 and GAMP5 (Good automated Manufacturing Practice) and we meet the French and European regulations relating 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), EolRandoTel© (randomisation by phone), web reporting (studies followed via internet) studies site (studies journal via internet).
EOL© is suitable for all types of medical and para-medical studies:
EOL© is addressed to all public and private research participants.
Institutional participants:
Private participants:
To download Medsharing's brochure in English, click here.
EOL New brochure available!
March 2016 : EOL the new brochure is available!
Medsharing in figures
(Figures 2015)
78,000 patients since 2003 for over 130 studies.
26 Registries / Observatories.
49 Studies.
61 Clinical Trials
31 Randomizations (without eCRF)
47 Drug Studies
28 DM Studies
66 Ongoing studies.
Figures 2015
New version of the application of randomization
Check out the new unlimited version of our Randomization for clinical trial application IPHONE / IPAD.
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