PharmaSUG2019paper·US·Submission Standards
Non-Clinical (SEND) Reference Guide for Clinical (SDTM) Programmers SS-317
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PharmaSUG2019paper·US·Submission Standards
How to use SUPPQUAL for specifying natural key variables in define.xml? SS-318
PharmaSUG2019paper·US·Submission Standards
A Standardized Data Sample: Key to Improving the Submission Strategy SS-331
PharmaSUG2019paper·US·Submission Standards
The Anatomy of Clinical Trials Data: A Beginner’s Guide SS-334
PharmaSUG2019paper·US·Submission Standards
Do-It-Yourself CDISC! A Case Study of Westat’s Successful Implementation of CDISC Standards on a Fixed Budget SS-337
PharmaSUG2019paper·US·Submission Standards
Panel Discussion: Recent Submission Experiences around the World SS-343
PharmaSUG2019paper·US·e-Posters
In the Style Of David Letterman’s “Top Ten” Lists, Our “Top Ten” PROC SQL Statements To Use in Your SAS Program PO-022
PharmaSUG2019paper·US·e-Posters
Advanced Project Management beyond Microsoft Project, Using PROC CPM, PROC GANTT, and Advanced Graphics PO-037
PharmaSUG2019paper·US·e-Posters
Put on the SAS® Sorting Hat and Discover Which Sort is Best for You! PO-050
PharmaSUG2019paper·US·e-Posters
Using Pinnacle 21 Enterprise for define.xml Creation: Tips and Tricks from a CRO Perspective. PO-066
PharmaSUG2019paper·US·e-Posters
Developing Analysis & Reporting Standards For Pharmaco-Epidemiology Observational Studies PO-108
PharmaSUG2019paper·US·e-Posters
Raw data sets tracker: Time and project management based on the volume of available clinical data using SAS® software PO-110
PharmaSUG2019paper·US·e-Posters
When biomarker drives primary endpoint: An oncology case study of SDTM design using multiple myeloma. PO-130
PharmaSUG2019paper·US·e-Posters
SDSP (Study Data Standardization Plan) Case Studies and Considerations PO-144
PharmaSUG2019paper·US·e-Posters
Why waiting longer to check log file when SAS program in Execution? Lets Find bugs Early!! PO-221