PharmaSUG2017paper·US·Data Integrity
Let’s Check Data Integrity Using Statistical (SAS®) Programmers with SAS® DA02
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PharmaSUG2017paper·US·Data Integrity
Conversion of CDISC specifications to CDISC data – specifications driven SAS programming for CDISC data mapping DA03
PharmaSUG2017paper·US·Data Integrity
Clinical and Vendor Database Harmony; Can’t we all just get along? DA05
PharmaSUG2017paper·China·Data Management & Validation
What's your data flow in LSAF (How to code in LSAF) DM-02 Shanghai
PharmaSUG2017paper·China·Data Management & Validation
How process flow standardized our process DM-04 Shanghai
PharmaSUG2017paper·China·Data Management & Validation
Strip Special & Non-Printable Characters in Your Data Set DM-05 Shanghai
PharmaSUG2017paper·US·Data Standards
The Untapped Potential of the Protocol Representation Model DS01
PharmaSUG2017paper·US·Data Standards
SDTM – Just a Walk in the (Theme) Park, Exploring SDTM in the Most Magical Place on Earth DS03
PharmaSUG2017paper·US·Data Standards
The CDISC Trial Design Model (TDM), the EPOCH variable, and the Treatment Emergent Flag: How to Leverage these to Improve Review DS04
PharmaSUG2017paper·US·Data Standards
Implementation of STDM Pharmacogenomics/Genetics Domains on Genetic Variation Data DS05
PharmaSUG2017paper·US·Data Standards
Harmonizing CDISC Data Standards across Companies: A Practical Overview with Examples DS06
PharmaSUG2017paper·US·Data Standards
Where Is the Link Broken – Another Look at SDTM Oncology Tumor Packages DS07
PharmaSUG2017paper·US·Data Standards
The CDISC SDTM Exposure Domains (EX & EC) Demystified. How EC Helps You Produce A Better (more compliant) EX. DS08