The module is used to produce the electronic CRF. It foresees online data validation, queries handling, 2-step data check and all the other basic and advanced functionalities of an EDC platform. Data are entered by the investigator or can be imported from external systems
No additional or specific software installation is requested on the user PCs. The only thing you need is a device connected to internet and your credential. All browsers and operating systems are supported.
A trial based on Clinical.net can be completely customizable both in terms of layout and internal processes in order to be compliant with the Sponsor needs and study protocols requirements
Clinical.net is able to import/export data from external system and to communicate with them for a complete management of the study, providing immediate feedback through the online reporting module
Randomization process is fully integrated within the page of the eCRF. The module allows the investigator to activate the procedure directly from the eCRF obtaining, immediately, all the information needed for this kind of process, such as randomization number, treatment arm, drug kit to be dispensed
The eLearning module is designed to train the platform users on the protocol, the system and on all other study specific procedures, and to provided them, after the completion of an online questionnaire, a valid certificate to be archived
This module, completely integrated into the Study Web Portal, is used to handle Protocol Deviation directly into the eCRF just like a standard query involving additional profiles such as Clinical Reviewer or Medical Monitor
Clinical.net is able to communicate with external system in order to import data into the database of the study or to export information in different formats. The connections are established via Web Services, API, flat text file or direct connection to the external data provider
Drug handling is one of the most important aspect in a lot of clinical study. This tool is used to handle the drug within the study. It is used both for logistic aspects and for compliance ones, ensuring users to have a real time overview of the entire process
The eSAE module is fully integrated with the eCRF and allows investigator to create a safety notification containing data from the eCRF and from the safety pages automatically merged within a PDF sent by email to the involved profiles.
Patient Reported Outcome and Patient Diaries can be now administered to the patients using our APP. It is completely integrated with the study web portal sharing the same database. It can be installed on patient’s device or provided already configured on a device handled by us.
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