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Best Practices in SAS Statistical Programming for Regulatory Submission

 
  June 06, 2011  
     
 
CfPA - The Center for Professional Advancement, Burlingame, CA
September 26-27, 2011


Who Should Attend
This course is intended for anyone directly or indirectly responsible for the creation, content or validation of summary tables, data lists and graphs used to support research, drug or medical device efficacy and safety in a regulatory submission. Professionals in the pharmaceutical, biotechnology and medical device industries who want to be 21 CFR Part 11 compliant in relation to the SAS programming environment will benefit from this unique course. Effective technical and practical solutions to address real-world issues will be provided.

This course is recommended for:
  • SAS Statistical Programmers
  • SAS Statistical Managers
  • Director, Statistical Programming
  • Statisticians
  • Clinical Data Managers
  • Quality Assurance Specialists
  • Medical Writers
  • Regulatory Affairs Associates
  • CRO Professionals
  • Health Care Professionals
  • Research Universities

Description
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.

 
 
Organized by: CfPA - The Center for Professional Advancement
Invited Speakers: Sunil Gupta; Senior SAS Consultant, Gupta Programming

Sunil Gupta, Senior Consultant, Gupta Programming. is a well known author, international SAS expert, speaker and consultant in the pharmaceutical industry for over 18 years. He has project management and hands-on programming experience of over eight successful FDA submissions with major pharmaceutical companies including Amgen, Pfizer and Isis Pharmaceuticals. Mr. Gupta has written the following popular books on SAS: Quick Results with SAS e-Guides, Quick Results with the Output Delivery System, Sharpening Your SAS Skills, and Data Management and Reporting Made Easy with SAS Learning Edition 2.0. In 2008, Mr. Gupta was selected as one of the top 100 Notable People in the Medical Device Industry. Mr. Gupta has over 50 SAS technical and industry-related publications.
 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: sberg@cfpa.com
 
   
 
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