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Conference Papers
13,885
available papers
10
available conferences
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PharmaSUG2016paper·US·Techniques and Tutorials
Beyond IF THEN ELSE: Techniques for Conditional Execution of SAS® Code TT16
PharmaSUG2016paper·US·Techniques and Tutorials
Capturing Macro Code when Debugging in the Windows Environment: The Power of MFILE and the Simplicity of Pasting TT17
PharmaSUG2016paper·US·Techniques and Tutorials
Duplicate records – it may be a good time to contact your data management team TT18
PharmaSUG SDE2016presentation·NC·A CDISC Grab Bag
SEND (The Standard for the Exchange of Nonclinical Data): History, Basics, and Comparisons with Clinical Data 01 North America · RTP, NC
PharmaSUG SDE2016presentation·NC·A CDISC Grab Bag
Associated Persons Domains – Who? What? Where? When? Why? How? 02 North America · RTP, NC
PharmaSUG SDE2016presentation·NC·A CDISC Grab Bag
The Protocol Representation Model: The Forgotten CDISC Model 03 North America · RTP, NC
PharmaSUG SDE2016presentation·NC·A CDISC Grab Bag
CDISC: Interoperability and Beyond… 04 North America · RTP, NC
PharmaSUG SDE2016presentation·NC·A CDISC Grab Bag
My Attempt to Rid the Clinical World of Excel 05 North America · RTP, NC
PharmaSUG SDE2016presentation·NC·A CDISC Grab Bag
ADaM Grouping: Groups, Categories, and Criteria. Which Way Should I Go? 06 North America · RTP, NC
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
Proper Parenting: A Guide in Using ADaM Flag/Criterion Variables and When to Create a Child Dataset 01 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
Using CDISC to Support the Healthy Birth, Growth & Development Knowledge Integration (Gates Foundation Project) 02 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
An Efficient Way to Create the SDTM TS Domain 03 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
DS- Disposition, the Role of One Domain 04 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
No USUBJID? No Problem!: Handling OpenCDISC Reports That Don’t Provide USUBJID 05 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
Applying SDTM and ADaM to the Construction of Datamarts in Support of Cross-indication Regulatory Requests 06 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
Some Sightings While Traveling the Road of ADaM Spec Review 07 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
Considerations in ADaM Occurrence Data: Handling Crossover Records for Non-Typical Analysis 08 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
Deconstructing ADRS: Tumor Response Analysis Data Set 09 North America · Chicago, IL
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and Feedback
To IDB or Not to IDB: That is the Question 10 North America · Chicago, IL