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Observational Studies

ShareCRF provides the capabilities to create and manage easily data from either your observational or clinical studies, also, allows adapting the trial to the changes produced over time.

ShareCRF is perfectly adapted to carry out with different kind of studies like observational studies, clinical trials and so on in a very easy, simple, economic and efficient way. The system allows to design and create the case report form as well as to manage multiple sites and investigators, allowing that each investigator only has access to the 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.