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"A considerable number of our early phase clinical trials have been managed with Promasys.
In Promasys, changes in the design of a trial, like when you add some new measurements, are immediately reflected in the CRF's, and are implemented throughout the study. Therefore you don't have to worry about the consistency of the trial, and that gives great flexibility, in the design phase of a trial, but also later on, for instance when amendments have to be implemented in the database.
One of the big advantages of Promasys for us is that the quality of the data is always very high, thanks to the functions in Promasys that support the reliability of the data. Data integrity is very well ensured through the intelligent and traceable access rights structure. In addition, it is very easy to export data to SAS, therefore the transfer of the data coming from Promasys to our own database always went very smoothly."
Dr. Pierre Peeters, Executive Director Clinical Pharmacology & Kinetics, Organon
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