| Starts: | Monday November 09, 2009 at 8:30am |
|---|---|
| Ends: | Friday November 13, 2009 at 5:00pm |
| Event Type: | Training/Seminar |
| Location: |
Courtyard by Marriott-Amsterdam Airport 2131 LX Hoofddorp Haarlemmermeer, NORTH HOLLAND 2131 NL |
| Price: | $ 1,640 ($ 1,840 after August 24, 2009) |
| Website: | http://www.cfpa.com/SortCourse.aspx?CourseID=2234&CSPlace=BOTH&CourseName=Best+Practices+in+SAS+Statistical+Programming+for+Regulatory+Submission&NoHref=1 |
| Industry: | pharmaceuticals |
| Keywords: | Clinical, Validation, Programming, Biotech, Research, Pharmaceutical, 21 Cfr Part 11, Proc Report, Ods, Sas, Fda |
| Intended For: | SAS Statistical Programmers, SAS Statistical Managers, Director, Statistical Programming, Statisticians, Clinical Data Managers, Quality Assurance Specialists, Medical Writers, Regulatory Affairs Associates, CRO’s, Health Care Professionals, Research Univ |
| Organization: | The Center for Profressional Advancement |
This intense 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.