PharmaSUG2013paper·US·Coders Corner
Useful Tips for Handling and Creating Special Characters in SAS® CC30
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Conference Papers
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PharmaSUG2013paper·US·Coders Corner
A Quick Patient Profile: Combining External Data with EDC-generated Subject CRF CC31
PharmaSUG2013paper·US·Coders Corner
Using SAS Driver Programs to Automate Workflows and Respond to the Unexpected CC34
PharmaSUG2013paper·US·Coders Corner
A One Line Method to Extract a Substring from a String using PRX CC35
PharmaSUG2013paper·US·Coders Corner
Turn Your Plain Report into a Painted Report Using ODS Styles CC37-SAS
PharmaSUG2013paper·US·Coders Corner
A Strategy to Ensure Non-Estimable Confidence Intervals Having Equal Lower and Upper Confidence Limits are Displayed Correctly CC38
PharmaSUG2013paper·US·Data Standards
Programming Validation Tips prior to using OpenCDISC validator DS03
PharmaSUG2013paper·US·Data Standards
Implementation Considerations for PARAM/PARAMCD Using ADaM BDS DS04
PharmaSUG2013paper·US·Data Standards
Building Traceability for End Points in Analysis Datasets Using SRCDOM, SRCVAR, and SRCSEQ Triplet DS05
PharmaSUG2013paper·US·Data Standards
Macro %D_ADSL – Automating ADSL Creation from Metadata File DS07
PharmaSUG2013paper·US·Data Standards
Data Standards Will Be Required: Challenges for Medical Device Submissions DS08
PharmaSUG2013paper·US·Data Standards
From Standards that Cost To Standards that Save: Cost Effective Standards Implementation DS09
PharmaSUG2013paper·US·Data Standards
Standardizing the Standards: A Road Map for Establishing, Implementing and Unifying Standards in Your Organization DS11
PharmaSUG2013paper·US·Data Standards
The Y2K17 Bug! Using Metadata to Respond to PDUFA V Requirements DS12
PharmaSUG2013paper·US·Data Standards
Experiences in Preparing Summary Level Clinical Site Data within NDA’s Submission for FDA’s Inspection Planning DS13