Best Practices in SAS Statistical Programming for Regulatory Submission Training Course :

Who Should Attend
Learning Objectives
Description
<strong>Course Schedule - March 26-27, 2009</strong><br/><br/>This<b> intense</b> two-day course focuses on the validation process to assure that correct, consistent and reliable summary tables are reproducible. In addition, a variety of effective methods for producing standard and custom summary tables will be provided. SAS data sets used in the course are CDISC ready. Discussions will focus on proven techniques to address real-world issues. Get your SAS technical and validation questions answered and learn efficient tips for producing a quality regulatory submission in a timely manner. Students will receive a CD containing all tools and SAS macros reviewed in the course.
12/10/2008 To 01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Pharmaceutical
Course Category
Brochure Name
http://www.cfpa.com/PDF/2009/2234,C8-185,0903-409.pdf
Address
New Brunswick, NJ USA