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

Who Should Attend
Learning Objectives
Description
<strong>Course Schedule - Pre-recorded Course</strong><br/><br/>This <b>intense</b> 90-minute <b><i>accreditied</b></i> online course focuses on the validation process to assure that correct, consistent and reliable summary tables are reproducible. 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<br><br> <b>Module 1: Analysis of potential setbacks</b> <ul><li>Identify potential delays and setbacks when creating and validating summary tables</li> <li>Develop plans to address these potential problems</ul></li> <b>Module 2: Developing a strategy in the QC Plan</b><ul><li> Understand the three levels of checks performed: Self, QC, & External QA</li> <li>Develop a game plan for risk management validation</ul></li> <b>Module 3: Effective methods and SAS macros to validate summary tables</b><ul><li> Understand the advantages of selected SAS procedures for validating tables</li> <li>Apply SAS macros to standardize the validation process</ul></li> <p><b>OTHER PARTS IN THIS SERIES:</b><br><br> <b>Part 2: <a href="http://www.cfpa.com/200805202214-15a/2214/t/2214/0/CourseSearch.aspx"target=_blank>Best Practices in SAS Statistical Programming for Regulatory Submission: Creating Publication-Quality Summary Tables </a></b> <br> <i>(Course Offering # 0805-406)</i><br><br> <br>Attend both parts and <b>SAVE $100</b> OR take either as a stand-alone course. Take both to maximize learning and minimize expense.<br><br><b></b><br><br>
01/13/2009 To 01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Pharmaceutical
Course Category
Brochure Name
http://www.cfpa.com/PDF/2008/2213,C8-098,0805-704.pdf
Address
AN ON-DEMAND ONLINE TRAINING FORMAT On-Demand Training