PharmaSUG2025Strategic Implementation & Innovation
An Introduction to the Role of Statistical Programming in Medical Affairs
Paper SI-359
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Conference Papers
Find papers in official PHUSE, PharmaSUG, and WUSS proceedings. Search by title or paper number, then narrow the directory by conference, year, or category.
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Showing 1076–1100 of 4,481 papers
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PharmaSUG2025Strategic Implementation & Innovation
Towards an Integrated Submission-Ready Data Pipeline: Unifying Compliance, Automation, and Open-Source Innovation
Paper SI-380
PharmaSUG2025Submission Standards
Identification of Domains Containing Screen Failure Participants in SDTMs and ADaMs for Reviewer’s Guides
Paper SS-070
PharmaSUG2025Submission Standards
A collaborative and agile approach for end to end Standards Governance and Release
Paper SS-087
PharmaSUG2025Submission Standards
PDFs Done Right: The Statistical Programmer’s Guide to Flawless Regulatory Submissions
Paper SS-127
PharmaSUG2025Submission Standards
Evaluation of the Process to Create CLINSITE define.xml: Macro Approach vs. ADCLIN Spec
Paper SS-135
PharmaSUG2025Submission Standards
Handling Health Regulatory Information Requests: Best Practices and Strategies
Paper SS-146
PharmaSUG2025Submission Standards
A Little Bit of This and That: Use cases, implementation, and documentation when using multiple CDISC standards, CTs, and regulatory guidances in an SDTM study
Paper SS-165
PharmaSUG2025Submission Standards
Key guidelines, Tricks and Experiences for PMDA and comparison with FDA and CDE submission
Paper SS-254
PharmaSUG2025Submission Standards
The Show Must Go On: Best Practices for Submitting SDTM Data for Ongoing Studies
Paper SS-258
PharmaSUG2025Submission Standards
Exploring the Upcoming Integrated cSDRG!
Paper SS-269
PharmaSUG2025Submission Standards
Updating Define-XML packages: Tips and A Comprehensive Checklist
Paper SS-276
PharmaSUG2025Submission Standards
ADaM and TFLs for Drug-induced Liver Injury (DILI) Analysis
Paper SS-306
PharmaSUG2025Submission Standards
Checking Outside the Box: A Framework for Submission Success
Paper SS-314
PharmaSUG2025Submission Standards
Leveraging previous study data for Extension studies: Structuring Subject and Participant Level Analysis datasets using CRF data
Paper SS-333
PharmaSUG2025Submission Standards
Ensuring Data Integrity: Techniques for Validating SDTM Datasets in Clinical Research
Paper SS-344
PharmaSUG2025Submission Standards
Common Issues in BIMO Clinical Site Dataset Packages
Paper SS-348
PharmaSUG2025e-Posters
ADaM implementation for Anti-drug Antibody Data
Paper PO-052
PharmaSUG2025e-Posters
A Macro to Automate Data Visualization using SAS Graph Template Language (GTL)
Paper PO-062
PharmaSUG2025e-Posters
Understanding HIV: At-Risk Populations, Treatment, Prevention and Standardized Data Representation in HIV Studies
Paper PO-095
PharmaSUG2025e-Posters
Checking SDTM Datasets from Biostatistical Perspective
Paper PO-133
PharmaSUG2025e-Posters
Considerations of R submission in Japan
Paper PO-140
PharmaSUG2025e-Posters
In-house Data Monitoring Committee Report Programming
Paper PO-172
PharmaSUG2025e-Posters
Our Second Brain: A Guide to Building Note System for SAS Programmer in Clinical Trial
Paper PO-208
PharmaSUG2025e-Posters
Embracing an Extra Step as the Ultimate Shortcut: Leveraging ADDATES for Enhanced Efficiency and Traceability in Oncology Studies
Paper PO-212