SAS Global Forum 2010, Pre-conference class
Instructor: Sunil Gupta, Director Statistical Programming, Quintiles
SAS programmers interested in learning and preparing for challenging careers in the pharmaceutical industry will benefit from this unique and in-depth course. Understanding the regulatory submission process and how you can contribute to assure correct and reproducible summary tables are essential. In addition, potential submission setbacks are analyzed to prevent delays using QC plan and risk-based management validation strategies. Finally, required documentation in SAS programs and validation checklists are reviewed to assure FDA regulatory compliance. Class discussions will focus on proven techniques to address real-world issues. Get your SAS technical and validation questions answered and learn efficiency tips for producing a quality regulatory submission in a timely manner.