Implementing CDISC Using SAS: An End-to-End Guide

For decades researchers and programmers have used SAS to analyze, summarize, and report clinical trial data. Now Chris Holland and Jack Shostak have written the first comprehensive book on applying clinical research data and metadata to the Clinical Data Interchange Standards Consortium (CDISC) standards.

Implementing CDISC Using SAS: An End-to-End Guide is an all-inclusive guide on how to implement and analyze Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) data and prepare clinical trial data for regulatory submissions. Topics covered include creating and using metadata, developing conversion specifications, implementing and validating SDTM and ADaM data, determining solutions for legacy data conversions, and preparing data for regulatory submission. The book covers products such as Base SAS, SAS Clinical Data Integration, and the SAS Clinical Standards Toolkit, as well as JMP Clinical.

Anyone dealing with CDISC standards including SAS or JMP programmers, statisticians, and data managers in the pharmaceutical, biotechnology, or medical device industries will find the philosophical best practices and implementation examples in this book invaluable.

• SAS Programming in the Pharmaceutical Industry, Second Edition
• Validating Clinical Trial Data Reporting with SAS (SAS Press)
• SAS Clinical Programming: In 18 Easy Steps
• Advanced SAS Interview Questions You'll Most Likely Be Asked
• Implementing CDISC Using SAS: An End-to-End Guide, Second Edition