PharmaSUG2023paper·US·Strategic Implementation & Innovation
An End-to-End and Fully Integrated Clinical Development Platform with eDC/Labs data Data Management, Medical Review, Statistical Analysis and Adaptive Design etc. SI-147
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PharmaSUG2023paper·US·Strategic Implementation & Innovation
SAS LOG/LST Filename improvement for easier: code review, code audit and project development history and chronology. SI-159
PharmaSUG2023paper·US·Strategic Implementation & Innovation
Introduction of AWS Cloud Computing and its future for Biometric Department SI-164
PharmaSUG2023paper·US·Strategic Implementation & Innovation
The implementation of Scrum in Pharmaceutical Data Analytics and Statistical Programming SI-170
PharmaSUG2023paper·US·Strategic Implementation & Innovation
Tips and traps on how to efficiently accelerate clinical trials to successful submission, approval, and launch SI-176
PharmaSUG2023paper·US·Strategic Implementation & Innovation
Making Multilingual Programmers – A Targeted Approach to R for Clinical Trials Training SI-202
PharmaSUG2023paper·US·Strategic Implementation & Innovation
R Package Qualification: Automation and Documentation in a Regulated Environment SI-212
PharmaSUG2023paper·US·Strategic Implementation & Innovation
Metaverse in the Healthcare – More Real than imagined! SI-227
PharmaSUG2023paper·US·Strategic Implementation & Innovation
Secret SAS – You Can Write eCTD Using ODS Word in SAS SI-235
PharmaSUG2023paper·US·Strategic Implementation & Innovation
PHUSE Safety Analytics Working Group – Overview and Deliverables Update SI-277
PharmaSUG2023paper·US·Strategic Implementation & Innovation
Auto-validation of SAS Macros through Regression Testing SI-302
PharmaSUG2023paper·US·Submission Standards
Handling CRS/NT Data in CAR-T Studies and Submission SS-003
PharmaSUG2023paper·US·Submission Standards
Optimizing Efficiency and Improving Data Quality through Meaningful Custom Fix Tips and Explanations SS-045
PharmaSUG2023paper·US·Submission Standards
CDISC Conformance and Compliance: So Many Resources, So Little Time! SS-059
PharmaSUG2023paper·US·Submission Standards
Study Data Technical Rejection Criteria (TRC) Considerations for Multiple Data Packages in a Single Submission SS-097
PharmaSUG2023paper·US·Submission Standards
Standardization of Reactogenicity Data into Findings SS-112
PharmaSUG2023paper·US·Submission Standards
Consistency Checks Automation across Regulatory Submission Documents in the eCTD M5 folder SS-117
PharmaSUG2023paper·US·Submission Standards
How Can I Put This? – Using a pre-defined spreadsheet to explain your Pinnacle 21 Enterprise Issues SS-124
PharmaSUG2023paper·US·Submission Standards
Proposal for New ADaM Paired Variables: PARQUAL/PARTYPE SS-127
PharmaSUG2023paper·US·Submission Standards
Working with Biomedical Concepts and SDTM Dataset Specializations for Define-XML using SAS© Open CST SS-140