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A proven methodology dedicated to e-CRF

MEDSHARING has developed a project methodology adapted to e-CRF to simplify its implementation and facilitate exchange with our customers throughout the design process right up to validation.

The following steps are conducted with careful planning and sequencing:

  • Audit of needs (exchange with the client about his project and developing his CRF);
  • eCRF supply preliminary model (general ergonomics and navigation in the eCRF);
  • Model validation by the customer (via a website dedicated to testing);
  • Data-handling supply to be completed by the client (Limits/Variable Name/Type/Length/Rules of coherence between the fields);
  • Terminal integration and installation of controls;
  • Final model supply for approval (via a website dedicated to testing);
  • Production start of the study on official go-ahead from the client (PV of beginning of production).

This last step leads to the official opening of the study with the provision of administrative codes for the creation of centres and investigators with the help of the administration console.

This methodology guarantees the supply of a quality project on time and within the budget agreed in our commitment.

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.

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by Neuro-Graph

July 2023

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