Validating Clinical Trial Data Reporting with SAS (SAS Press)

By Carol Matthews, Carol I. Matthews, Brian C. Shilling

Book Overview

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 (FDA). The authors provide practical examples and tips for avoiding errors in your output.

• Format: Paperback
• Language: English
• ISBN: 1599941287
• ISBN13: 9781599941288
• Release Date: March 2008
• Publisher: SAS Institute
• Length: 224 Pages
• Weight: 4.75 lbs.
• Dimensions: 0.4" x 7.5" x 8.9"

Customer Reviews

Sorely needed book! Big Pharma, please buy this book for your employees!

As a programmer in the pharmaceutical community, I have been waiting years for a book like this. Validating data for clinical trials is crucial to not only portraying the data accurately but also to save money! I believe that pharmaceutical companies should purchase this book for each and every employee who works in or around clinical data.