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The Center for Professional Advancement, An Online Training Format
May 20, 2008
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 with effective and practical solutions to address real-world issues will benefit from this unique course. - SAS Statistical Programmers
- Critical Path Personnel
- SAS Statistical Managers
- Statisticians
- Clinical Data Managers
- Quality Assurance Specialists
- Medical Writers
- Regulatory Affairs Associates
- Director, Statistical Programming
Description
This intense 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.
Module 1: Process Flow for developing summary tables (CL) - Prepare the data structure and variables
- Extract descriptive statistics using SAS’s Output Delivery System
- Assemble and summarizing reporting SAS data set
Module 2: Effective methods and SAS macros to create summary tables - Understand the benefits of effective methods for creating tables
- Apply SAS macros to standardize the production process
Module 3: Anatomy of Proc Report, ODS and RTF Control Words - Customization and flexibility with Proc Report, ODS and RTF Control Words
- Standardization with SAS’s Style Definitions
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Organized by:
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The Center for Professional Advancement |
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Invited Speakers:
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Sunil Gupta, Associate Director, Statistical Programming, Quintiles Inc., International SAS Expert, Speaker, Trainer and Author
Sunil Gupta has been an Independent Consultant since July 1994. He became a SAS Institute Quality Partner the following year. In 2000, he became a SAS Certified Professional V6 and in 2003 he passed the SAS Base Programmer Certification exam. During his 14 years experience in the Biomedical, Pharmaceutical, Biotech and Sales & Marketing Industries, Mr. Gupta has been in management and project lead positions. He understands how business functions and how to work together as a team member to achieve results. Mr. Gupta has developed and taught many topics related to SAS skills and has done numerous presentations and workshops at SUGI, Regional and Local SAS User Groups meetings. He has authored and co-authored on this topic. In 2006, he released his third SAS book titled “Data Management and Reporting Made Easy with SAS Learning Edition 2.0”.
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Deadline for Abstracts:
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n/a
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Registration:
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Please click here for registration information.
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E-mail:
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ino@cfpa.com
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