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Validating Clinical Trial Data Reporting with SAS

Autor Carol I. Matthews, Brian C. Shilling
en Limba Engleză Paperback – 22 mar 2008
Validation is a critical component to programming clinical trial analysis. Essential to effective validation is the programmer's understanding of the data with which they'll be working. If you don't understand how the data is arranged, the values that are reasonable for each variable, and the way the data should behave, you cannot ensure that the final result of your programming effort is complete or even appropriate. Therefore, to be a successful programmer in the pharmaceutical industry, you need to understand validation requirements and to learn how to make the code do the bulk of the work so that your programs are efficient as well as accurate.
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Specificații

ISBN-13: 9781599941288
ISBN-10: 1599941287
Pagini: 224
Ilustrații: 1
Dimensiuni: 191 x 235 x 13 mm
Greutate: 0.43 kg
Editura: SAS Institute Inc.

Descriere

This indispensable guide focuses on validating programs written to support the clinical trial process from after the data collection stage to generating reports and submitting data and output to the Food and Drug Administration.