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IVRS
PSI has launched its own IVRS service to support multi-center clinical trials. Our system is capable of accommodating 2,000 callers, provides our clients with real-time data on the progress of their study, and it takes less than one minute to log each subject visit.
IVRS…
Provides a solution to the problem of over-enrollment
When target enrollment has been reached, IVRS will not allow any more subjects to be registered. This rules out the possibility of over-enrollment and the associated costs.
Offers up-to-the-minute reports
As soon as subject information has been logged via the IVR telephone system, the details are immediately transmitted to our tracking database, to give our clients access to the most up-to-date data possible.
Allows tracking of study progress in real-time
Clients who follow their study via the internet will receive the extra benefit of being able to view their study enrollment, randomization and visits in real-time, as investigators enter the information.
Keeps track of study drug requirements at sites
Once the investigator has logged a randomization, and IVRS has assigned the study drug to the subject, it immediately – and automatically – sends an order to the regional warehouse for the allocated drug to be delivered to the site.
Provides significant advantages for investigators
IVRS is simple to use, and faster than filling in forms, but maintains the same level of data quality. In addition, IVRS is recorded in the native languages of our investigators.
PSI's IVRS is an indispensable tool for our clients to keep track of their clinical trials.
IVRS…
Provides a solution to the problem of over-enrollment
When target enrollment has been reached, IVRS will not allow any more subjects to be registered. This rules out the possibility of over-enrollment and the associated costs.
Offers up-to-the-minute reports
As soon as subject information has been logged via the IVR telephone system, the details are immediately transmitted to our tracking database, to give our clients access to the most up-to-date data possible.
Allows tracking of study progress in real-time
Clients who follow their study via the internet will receive the extra benefit of being able to view their study enrollment, randomization and visits in real-time, as investigators enter the information.
Keeps track of study drug requirements at sites
Once the investigator has logged a randomization, and IVRS has assigned the study drug to the subject, it immediately – and automatically – sends an order to the regional warehouse for the allocated drug to be delivered to the site.
Provides significant advantages for investigators
IVRS is simple to use, and faster than filling in forms, but maintains the same level of data quality. In addition, IVRS is recorded in the native languages of our investigators.
PSI's IVRS is an indispensable tool for our clients to keep track of their clinical trials.