Complimentary White Paper
End-to-end clinical data management involves setting up specifications for clinical trial data once during the lifetime of the clinical trial, and being able to reuse the data structure to produce standards-based information – from the point when patient data is captured in the clinic all the way to when the analysis report is in the hands of regulatory authorities and the pharmaceutical sponsor.
This white paper explains the revolutionary steps being taken to achieve the objective of end-to-end clinical data management: spending less time on operational data management activities and more time on data exploration and analysis. Read about how bringing together integrated, well-documented clinical data will lead to shorter trials, improve the modeling of new trials before the therapy is tested on patients, and result in higher-quality drug submissions to authorities.
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