PharmaSUG2025paper·US·Submission Standards
Key guidelines, Tricks and Experiences for PMDA and comparison with FDA and CDE submission SS-254
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PharmaSUG2025paper·US·Submission Standards
The Show Must Go On: Best Practices for Submitting SDTM Data for Ongoing Studies SS-258
PharmaSUG2025paper·US·Submission Standards
Updating Define-XML packages: Tips and A Comprehensive Checklist SS-276
PharmaSUG2025paper·US·Submission Standards
ADaM and TFLs for Drug-induced Liver Injury (DILI) Analysis SS-306
PharmaSUG2025paper·US·Submission Standards
Checking Outside the Box: A Framework for Submission Success SS-314
PharmaSUG2025paper·US·Submission Standards
Leveraging previous study data for Extension studies: Structuring Subject and Participant Level Analysis datasets using CRF data SS-333
PharmaSUG2025paper·US·Submission Standards
Ensuring Data Integrity: Techniques for Validating SDTM Datasets in Clinical Research SS-344
PharmaSUG2025paper·US·Submission Standards
Common Issues in BIMO Clinical Site Dataset Packages SS-348
PharmaSUG2025paper·US·e-Posters
A Macro to Automate Data Visualization using SAS Graph Template Language (GTL) PO-062
PharmaSUG2025paper·US·e-Posters
Understanding HIV: At-Risk Populations, Treatment, Prevention and Standardized Data Representation in HIV Studies PO-095
PharmaSUG2025paper·US·e-Posters
Our Second Brain: A Guide to Building Note System for SAS Programmer in Clinical Trial PO-208
PharmaSUG2025paper·US·e-Posters
Embracing an Extra Step as the Ultimate Shortcut: Leveraging ADDATES for Enhanced Efficiency and Traceability in Oncology Studies PO-212
PharmaSUG2025paper·US·e-Posters
From Tides to Transformation: Making Waves with Your Move to Viya PO-236
PharmaSUG2025paper·US·e-Posters
Methodology for AI-driven Outcome Prediction for Patients with Atrial Fibrillation After Transcatheter Aortic Valve Implantation (TAVI) PO-252