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Clinical Trials

ShareCRF is the perfect tool for data management of any clinical trial phase (I, II, III, IV) in a safe, quick and simple way.

ShareCRF is perfectly adapted to carry out the management of the data of any kind of clinical trial(Phase I, II, III and IV) in a very easy, simple, economic and efficient way. The system allows having a shared CRF design between every site participating in the study, having each site access to only its own data (Data entered by them).

ShareCRF facilitates the task to the pharmaceutical industry and CRO’s, in addition to the coordination between both, allowing to manage the changes that happen in the CRF over time to adapt to different needs. Also managing the registration of new users, the different types of users with different types of permissions (users, test users, coordinators, colaborators in the CRF edition, promoters, sponsors), and then define the access permissions of each one of them, for the system to adapt to their requirements.