PharmaSUG2025paper·US·e-PostersAvoiding the Ouch: Mastering Time to Pain Progression Analysis PO-261See metadata
PharmaSUG2025paper·US·e-PostersStreamlining Your Workflow: Creating Portable and Automated SAS® Enterprise Guide Project Using Project Name PO-271See metadata
PharmaSUG2025paper·US·e-PostersAutomating Recurring Data Reconciliation for Serious Adverse Events Using SAS PO-274See metadata
PharmaSUG2025paper·US·e-PostersStatistical Programming Outputs Comparison and Reporting Using Python PO-311See metadata
PharmaSUG2025paper·US·e-PostersA Novel ADEFF Design with Varying Baseline Type Selections PO-350See metadata
PharmaSUG2025paper·US·e-PostersEfficient Strategies for Handling Data Issues in Clinical Trial Submissions PO-361See metadata
PharmaSUG2025paper·US·e-PostersSlamming Datasets Together, Without Hurt, Using SAS, R and Excel PO-366See metadata
PharmaSUG2025paper·US·e-PostersThe World is Not Enough: Base SAS Visualizations and Geolocations PO-382See metadata
PharmaSUG2025paper·US·e-PostersExCITE-ing! Build Your Paper’s Reference Section Programmatically Using Lex Jansen’s Website and SAS PO-391See metadata
PharmaSUG2025paper·US·e-PostersAssociation of Alzheimer’s Disease with Cardiovascular Disease and Depression in Older Adults: Findings from the 2018 Nationwide Inpatient Sample PO-402See metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Keynote: The Evolution of Statistical Programmers in a Dynamic Regulatory Industry 01 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!An Implementation of PK-QT Analysis 02 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Implementing Best Practices for Clinical Data Standards in Modern Digital Era for Regulatory Submissions 03 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Automating Clinical Study Report Development Using Generative AI 04 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Enhanced Kaplan-Meier Plots with ggplot2: Integration of At-Risk and Statistics Tables in R 05 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Advancing Clinical Trial Submissions: The Impact of GenAI and CDISC Compliance with Trustworthy Analytics 06 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Real-World Evidence (RWE) – Transforming Healthcare Decision-Making 07 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Unveiling Hidden Insights: Leveraging Knowledge Graphs for Precision Medicine and Clinical Data Analysis 08 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!Creating an SDTM Chatbot (P21) in MS Teams 09 Asia-Pacific · Hyderabad, IndiaSee metadata
PharmaSUG SDE2025paper·India·Clinical Data Standards and Technology: Gateway to Regulatory Submissions!An Overview of Regulatory Submission by Using R Language 10 Asia-Pacific · Hyderabad, IndiaSee metadata