Description
<strong>Course Schedule - Pre-recorded Course</strong><br/><br/>This<b> intense</b> 90-minute online course focuses on the variety of effective methods for producing standard and custom summary tables. 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: Process Flow for developing
summary tables (CL)</b><ul>
<li>Prepare the data structure and
variables</li>
<li>Extract descriptive statistics using
SAS’s Output Delivery System</li>
<li>Assemble and summarizing reporting
SAS data set</ul></li>
<b>Module 2: Effective methods and SAS
macros to create summary tables</b><ul>
<li>Understand the benefits of effective
methods for creating tables</li>
<li>Apply SAS macros to standardize the
production process</ul></li>
<b>Module 3: Anatomy of Proc Report,
ODS and RTF Control Words</b><ul>
<li>Customization and flexibility with Proc
Report, ODS and RTF Control Words</li>
<li>Standardization with SAS’s Style Definitions</ul></li>
<p><b>OTHER PARTS IN THIS SERIES:</b><br><br>
<b>Part 1: <a href="http://www.cfpa.com/190001012213-16a/2213/o/courseSummary.aspx"target=_blank>Best Best Practices in SAS Statistical Programming for Regulatory Submission: Understanding and Applying the QC Plan to Validate Summary Tables</a></b> <br> <i>(Course Offering # 0805-704)</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>
12/10/2008
To
01/01/0001
Training Company
The Center for Professional Advancement (CfPA)
Industry
Biotech
Course Category
Brochure Name
http://www.cfpa.com/PDF/2008/2214,C8-100,0806-701.pdf
Address
AN ON-DEMAND ONLINE TRAINING FORMAT On-Demand Training