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Cost Control - Risk Mgmt. White Papers

Life Sciences Solutions: Clinical Development

Overview In order to be compliant with FDA regulations, clinical modeling teams must maintain detailed records about the processes used to model drug effects prior to trials. Data must be submitted detailing how jobs were run and specifying the applications and systems used to run them. Biostatisticians working with population data to model a drug's effects on a patient can significantly shorten simulation runtimes by using Grid MP-enabled applications - analyzing thousands of dose concentration effect models in a fraction of previous timeframes.

Further White Paper Details
Publisher	United Devices	File Format	PDF, requires Acrobat Rdr 5
Date Published	November 2004	Downloads	1
Format	Case Studies
Topics	Cost Control - Risk Mgmt., High Performance Computing

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