PharmaSUG2024paper·US·Strategic Implementation & Innovation
PHUSE Safety Analytics Working Group – Overview and Deliverables Update SI-291
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PharmaSUG2024paper·US·Strategic Implementation & Innovation
A Change is Gonna Come: Maintaining Company Culture, Managing Time Zones, and Integrating Teams after a Global Acquisition SI-319
PharmaSUG2024paper·US·Strategic Implementation & Innovation
aCRF Copilot: Pioneering AI/ML Assisted CRF Annotation for Enhanced Clinical Data Management Efficiency SI-346
PharmaSUG2024paper·US·Strategic Implementation & Innovation
SASBuddy: Enhancing SAS Programming with Large Language Model Integration SI-362
PharmaSUG2024paper·US·Strategic Implementation & Innovation
Facilitating Seamless SAS-to-R Transition in Clinical Data Analysis: A Finetuned LLM Approach SI-391
PharmaSUG2024paper·US·Strategic Implementation & Innovation
Agile Sponsor Oversight of Statistical Programming Activities SI-408
PharmaSUG2024paper·US·Strategic Implementation & Innovation
One size does not fit all: The need and art of customizing SCE and MDR for end users SI-446
PharmaSUG2024paper·US·Strategic Implementation & Innovation
Embracing Diversity in Statistical Computing Environments: A Multi-Language Approach SI-452
PharmaSUG2024paper·US·Submission Standards
BIMO Brilliance: Your Path to Compliance Resilience SS-132
PharmaSUG2024paper·US·Submission Standards
Cultivating Success with Non-standard Investigator-sponsored Trial Data for FDA Submissions SS-133
PharmaSUG2024paper·US·Submission Standards
Is a Participation-Level ADaM Dataset a Solution for Submitting Integration Data to FDA? SS-213
PharmaSUG2024paper·US·Submission Standards
Creating Adverse Event Tables using R and SASSY System SS-263
PharmaSUG2024paper·US·Submission Standards
Combine PDFs in Submission-ready Format Quick and Easy SS-290
PharmaSUG2024paper·US·Submission Standards
Leveraging SAS and Adobe Plug-in for CRF Bookmark Generation (Rave studies) SS-306
PharmaSUG2024paper·US·Submission Standards
How to generate a submission ready ADaM for complex data SS-311
PharmaSUG2024paper·US·Submission Standards
Lead-in and extension trials, how we documented datapoint traceability SS-333
PharmaSUG2024paper·US·Submission Standards
Piloting into the Future: Publicly available R-based Submissions to the FDA SS-344
PharmaSUG2024paper·US·Submission Standards
A Programmer’s Insight into an Alternative to TQT Study Data Submission SS-363
PharmaSUG2024paper·US·Submission Standards
Design Considerations for ADaM Protocol Deviations Dataset in Vaccine Studies SS-368