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
Official-source directory
Conference Papers
13,885
available papers
10
available conferences
Papers
Showing 3181–3200 of 13,885
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
PharmaSUG2024paper·US·Submission Standards
Experimenting with Containers and webR for Submissions to FDA in the Pilot 4 SS-376
PharmaSUG2024paper·US·Submission Standards
Challenges and Considerations When Building e-Submission SDTM Data Packages SS-377
PharmaSUG2024paper·US·Submission Standards
Submitting Patient-Reported Outcome Data in Cancer Clinical Trials- Guidance for Industry Technical Specifications Document SS-422
PharmaSUG2024paper·US·e-Posters
Enhancing Define-XML Generation: Based on SAS Programming and Pinnacle 21 Community PO-123
PharmaSUG2024paper·US·e-Posters
A Deep Dive into Enhancing SAS/GRAPH® and SG Procedural Output with Templates, Styles, Attributes, and Annotation PO-128