EOL©, an e-CRF solution for clinical studies and randomization

EOL© a solution adapted to your profile

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Ideal communication

eCRF can simplify the exchange of information and optimise communication between participants.

eCRF unites all participants in the study around a single tool:

  • People authorised to enter data (Investigators, CSTs, Study Nurses);
  • People entitled to monitor the data (CRAs, Data Managers);
  • People authorised to monitor the study (Project Manager, Sponsors).

EOL© provides users with means of communication:

  • Notifications for inclusions, randomisation, EIGs, protocol deviations ... ;
  • Notifications on requests for correction;
  • Private messaging, encrypted to communicate between users;
  • Access to study documentation (protocol, Quality of Life Questionaires, Inform Consent ...);
  • Shared real-time reporting (table of inclusions, curves, list of centres ...);
  • Alerts during unblinding, processing allocation, mini stock, in a centre.

EOL animation

Our news

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.

Contact Medsharing

+33 (0)1 48 75 39 14
by e-mail

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by Neuro-Graph

June 2017

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