PharmaSUG2017paper·US·Submission Standards
The Do’s/Don’ts, An SDTM Validation Perspective. The should/shouldn’t when explaining issues in the Study Data Reviewers Guide SS10
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PharmaSUG2017paper·US·Submission Standards
Documenting Traceability for the FDA: Clarifying the Legacy Data Conversion Plan & Introducing the Study Data Traceability Guide SS11
PharmaSUG2017paper·US·Submission Standards
Quality Check your CDISC Data Submission Folder Before It Is Too Late! SS12
PharmaSUG2017paper·US·Techniques & Tutorials
Building Intelligent Macros: Using Metadata Functions with the SAS® Macro Language TT02
PharmaSUG2017paper·US·Techniques & Tutorials
Check Please: An Automated Approach to Log Checking TT06
PharmaSUG2017paper·US·Techniques & Tutorials
Converting Non-Imputed Dates for SDTM Data Sets With PROC FCMP TT07
PharmaSUG2017paper·US·Techniques & Tutorials
Clinical Trials Data: It’s a Scary World Out There! or Code that Helps You Sleep at Night TT08
PharmaSUG2017paper·US·Techniques & Tutorials
Hashtag #Efficiency! An Exploration of Hash Tables and Other Techniques TT09
PharmaSUG2017paper·US·Techniques & Tutorials
Data Quality Control: Using High Performance Binning to Prevent Information Loss TT10
PharmaSUG2017paper·US·Techniques & Tutorials
Application of Deming Regression in Molecular Diagnostics using a SAS® Macro TT12
PharmaSUG2017paper·US·Techniques & Tutorials
Defensive Programming — Tips and Techniques for Producing that Dataset, Table, Listing or Figure First Time TT14
PharmaSUG2017paper·US·Techniques & Tutorials
Merge With Caution: How to Avoid Common Problems when Combining SAS Datasets TT15
PharmaSUG2017paper·US·Techniques & Tutorials
Dear Dave, Please See the .LST File for Our Validation Differences. Thanks, Bad Validation Programmer TT16
SAS Global Forum2017paper·All Papers
Sankey Diagram: A Compelling, Convenient, and Informational Path Analysis with SAS® Visual Analytics 0135-2017 North America