PharmaSUG2019paper·China·Data Management & Validation
Case Study: Using Base SAS to Automate Quality Checks of Excel Workbooks that have Multiple Worksheets DM-40 Shanghai
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PharmaSUG2019paper·China·Data Management & Validation
Medical Review Support in Clinical Trial: Method of Staging Lung Cancer Automatically According to TNM Staging System Using SAS Software DM-42 Shanghai
PharmaSUG2019paper·China·Data Management & Validation
A User-Customized and Automatic SDTM Data Checking Tool DM-45 Shanghai
PharmaSUG2019paper·China·Data Management & Validation
Creating a Function for Lab Toxicity Grading using PROC FCMP DM-48 Shanghai
PharmaSUG2019paper·China·Data Management & Validation
Top 10 SAS programming efficiencies DM-81 Shanghai
PharmaSUG2019paper·US·Data Standards
Streamlining the Metadata Management Process Using SAS® Life Science Analytics Framework DS-049
PharmaSUG2019paper·US·Data Standards
Strategy to Evaluate the Quality of Clinical Data from CROs DS-087
PharmaSUG2019paper·US·Data Standards
Pacemaker Guy: De-Mystifying a Business Use Case for SDTM Standard and Medical Device Domains DS-088
PharmaSUG2019paper·US·Data Standards
Common Pinnacle 21 Report Issues: Shall we Document or Fix? DS-119
PharmaSUG2019paper·US·Data Standards
Considerations when Representing Multiple Subject Enrollments in SDTM DS-146
PharmaSUG2019paper·US·Data Standards
Bidirectionality to LOINC: Handling the Nitty Gritty of Lab Data DS-151
PharmaSUG2019paper·US·Data Standards
Leveraging Intermediate Data Sets to Achieve ADaM Traceability DS-185
PharmaSUG2019paper·US·Data Standards
Practical Guide for Creating ADaM Datasets in Cross-over Studies DS-196
PharmaSUG2019paper·US·Data Standards
This Paper focuses on CDISC Questionnaires, Ratings and Scales (QRS) supplements and types of FDA Clinical Outcome Assessments DS-202
PharmaSUG2019paper·US·Data Standards
Homogenizing Unique and Complex data into Standard SDTM Domains with TAUGs DS-223