iClinica comes loaded with features that are truly intelligent. The features empower the subscribers to complete the study quickly and reliably. The features have been developed with insight into the methodology and process of studies to ensure complete leveraging.


The system allows the investigator to screen subjects for participation in the study. During the process of screening the system ensures that the site caps and the study caps for screening are adhered to.


The systems allows for the enrolment of a successfully screened subject into the study. During the process of enrolling the subject, the system ensures that the enrolment caps, if any, at the site or study level, are adhered to. Moreover, the system verifies that the subject can be randomized and if there are issues flag it during enrolment itself so that the investigator can take an appropriate decision.


The system enables the user to perform run-in visits for trials. The user can easily configure the schedule of the run-in while also configuring if the run-in drug needs to be dispensed. The system has the ability to dispense a run-in drug to the subject if required.


The system allows the bio-statisticians to create, review, approve and monitor the lists for the study. The system further allows for the trial biostatician to get the patient data to verify randomization and drug assignment.


Randomization is a clinical trial design strategy used to assign participants to an arm of a study as defined in the protocol. The system supports multiple forms of randomization studies such as parallel, cohorts, cross-over, open-label, single-blinded, double-blinded and triple-blinded. The system allows checking of randomization caps at the site and study level during this process. The system also provides for dispensing of the study drug during randomization.


The system is equipped with the ability to define the drugs to be assigned to subjects on randomization and ensures that the correct drug is dispensed based on the randomization scheme.


The system supports washout visits and ensures that appropriate drugs are dispensed during visits. The system enables the end user to define a washout prior to randomization at the end of the trial and also configure a wash out visit at the time of cross-over.


The system allows you to define all the visits, their order and duration in a study. This enables you to create a visit template for the study which can be used to track the orderly visits for each subject. The system also offers the provision to map the various visits and the study day on which they occur.


The system allows you to create and maintain the kit list depending on the study configuration. The system interfaces with industry standard statistical tools for the generation of the same. The user can then review the generated list and load them into the system. The user can choose to load an externally generated list into the system.


The system supports unplanned visits like discontinue, break-blind, remove-hold, on-hold for subject and kit re-dispensing.


The system supports multiple reports which are comprehensive and easily interpretable in nature. These reports allow the stakeholders to make quick decisions to impact the efficiency of operations.


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