Collecting, managing, standardizing and analyzing clinical data during (and after) a clinical trial is crucial in the process for submission and regulatory approval of a new compound, biological, device or other therapy. A central clinical platform requires: Robust and auditable analytics to prove the result to the authorities and external
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Three things you must do to create a central clinical platform
Let SAS® Studio do your clinical research ‘tasks’
SAS is widely used in clinical research activities including: Managing and transforming data. Generating tabular and graphical summaries. Performing powerful statistical analyses such as safety and efficacy evaluations. In addition, SAS provides a number of interfaces from which a user can select to work with the data. One of these
Let SAS® Studio do your clinical research ‘tasks’
SAS is widely used in clinical research activities including: Managing and transforming data. Generating tabular and graphical summaries. Performing powerful statistical analyses such as safety and efficacy evaluations. In addition, SAS provides a number of interfaces from which a user can select to work with the data. One of these