PHUSE2026Emerging Trends & Open Source Technologies
RADAR: Rapid AGILE Development and Automated Reporting for Clinical Data Standards (Using an R Shiny-Based Application)
Paper ET08
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Conference Papers
Find papers in official PHUSE, PharmaSUG, and WUSS proceedings. Search by title or paper number, then narrow the directory by conference, year, or category.
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Showing 126–150 of 4,481 papers
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PHUSE2026Emerging Trends & Open Source Technologies
RIP – Inconsistent Metadata Specifications with RAP (R And Python). Generate Specs Faster and Detect Early Errors to Speed Up Submissions
Paper ET09
PHUSE2026Emerging Trends & Open Source Technologies
Open-Source Frameworks for Scalable Data Quality Orchestration in Clinical Data Pipelines
Paper ET10
PHUSE2026Emerging Trends & Open Source Technologies
ValoRpacks – Self-Service R Package Validation
Paper ET12
PHUSE2026Emerging Trends & Open Source Technologies
Accelerating Regulatory Submissions with R: A Scalable and Compliant Approach
Paper ET13
PHUSE2026Emerging Trends & Open Source Technologies
Unveiling Powerful Patient Data Insights Through Graph Databases
Paper ET15
PHUSE2026Industry Standards
Building High-Quality SDTM from Real-World Data: Lessons and Solutions
Paper DS06
PHUSE2026Industry Standards
Not Another Other: Bridging Data Collection with SDTM Mapping Without Open Text Fields
Paper DS10
PHUSE2026Industry Standards
Standardising Exposure-Response Data for Modelling and Simulation Using CDISC Principles and {admiral}
Paper DS12
PHUSE2026Industry Standards
CDISC Biomedical Concepts for Breast Cancer: A CDISC 360i Perspective
Paper DS17
PHUSE2026Industry Standards
Metadata-Driven TFL Generation: End-to-End Automation from Protocol to Output
Paper DS18
PHUSE2026Industry Standards
From System Exports to Standards: Will Standardisation of External Vendor Data Redefine Clinical Data Management/Analysis?
Paper DS19
PHUSE2026Industry Standards
Transforming Legacy Data into CDISC Standards: Practical Approaches and Regulatory Insights
Paper DS20
PHUSE2026Industry Standards
Optimising Trial Design Dataset Creation To Minimise P21 Compliance Issues
Paper DS22
PHUSE2026Industry Standards
From Data to Dossier: Lessons from Cross-Company Regulatory Submissions
Paper SA01
PHUSE2026Industry Standards
Breaking Free from the xpt: Exploration of Dataset-JSON as an Alternative Transport File to Regulatory Agencies
Paper SA02
PHUSE2026Industry Standards
Acquiring a Compound with Multiple Clinical Trials? Let’s Get Ready for a Type C Meeting! Key Considerations for Preparing Its Regulatory Submission
Paper SA03
PHUSE2026Industry Standards
Trends in eSub Evaluation Findings: A Twenty-Year Perspective on Data Traceability
Paper SA04
PHUSE2026Industry Standards
Electronic Submission of Population PK Analysis Files… What’s Your Modus Operandi?
Paper SA05
PHUSE2026Industry Standards
Submitting eCRT SDTM Data for ISS
Paper SA06
PHUSE2026Industry Standards
Common Issues in BIMO Clinical Site Dataset Packages
Paper SA07
PHUSE2026Industry Standards
Key Guidelines, Tricks and Experiences for the PMDA and a Comparison with FDA and NMPA CDE Submissions
Paper SA08
PHUSE2026Industry Standards
Multi-Standard Submission – Process, Learnings and Recommendations for Best Practice
Paper SA09
PHUSE2026Industry Standards
From Legacy to ISS/ISE: Real-World Lessons in Module 5 Submissions
Paper SA10
PHUSE2026Industry Standards
Building Cross-Functional Regulatory and Programming Alignment for Successful Submissions
Paper SA11