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Data Management in Analyzing Clinic Trial Data - Metadata Application
Overview Efficiently handling Clinical Trial Data based on the Clinical Data Interchange Standards Consortium (CDISC) standard, the regulatory rules from U.S. Food and Drug Administration (FDA) and electronic data submission requirements is very important for Drug Development. Effectively managing Clinical Trial data can vastly increase work efficiency and reduce the probability and introduction of mistakes. The data handling procedure presented here is based on several years of practical working experiences - coupling a metadata application tool on the desktop and specialized SAS macros to apply the metadata to satisfy this need.
| Publisher | SAS Institute | File Format | |
|---|---|---|---|
| Date Published | April 2004 | ||
| Format | White Papers | ||
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