PharmaSUG2016paper·China·Data Analysis, Statistics
Using SAS to Calculate Statistical Properties of Traditional 3+3 Design DS-08 Beijing
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PharmaSUG2016paper·US·Data Standards
Tips and tricks when developing Trial Design Model Specifications that provide Reductions in Creation time DS02
PharmaSUG2016paper·US·Data Standards
“It is a standard, so it is simple, right?”: Misconceptions and Organizational Challenges of Implementing CDISC at a CRO DS06
PharmaSUG2016paper·US·Data Standards
Considerations and Conventions within the Therapeutic Area User Guides (TAUGs) DS07
PharmaSUG2016paper·US·Data Standards
Prepare for Re-entry: Challenges and Solutions for Handling Re-screened Subjects in SDTM DS09
PharmaSUG2016paper·US·Data Standards
Associated Persons Domains – Who? What? Where? When? Why? How? DS10
PharmaSUG2016paper·US·Data Standards
Conformance, Compliance, and Validation: An ADaM Team Lead’s Perspective DS12
PharmaSUG2016paper·US·Data Standards
Implementation of ADaM Basic Data Structure for Cross-over Studies DS13
PharmaSUG2016paper·US·Data Standards
Codelists Here, Versions There, Controlled Terminology Everywhere DS16
PharmaSUG2016paper·China·Data Visualization
Change mindset: Review the data based on visualization DV-02 Beijing
PharmaSUG2016paper·China·Data Visualization
How to make GTL programming easy - An introduction to a GTL macro DV-03 Beijing
PharmaSUG2016paper·China·Data Visualization
The NextGEN of Lumberjacks: Are You Using the Right Tool For the Right Tree in the Forest? DV-04 Beijing