PHUSE2025Data Visualisation (DV)
Cracking the Curve: Unlocking Clinical Insights with Ridgeline Plots
Paper DV06
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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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PHUSE2025Data Visualisation (DV)
Interactive Insights: Leveraging R Shiny for Enhanced Data Visualisation in Clinical Trial Readouts
Paper DV07
PHUSE2025Data Visualisation (DV)
Visualising the Invisible: Patient Journey with Waterfall, Spider and Swimmer Plots
Paper DV08
PHUSE2025Data Visualisation (DV)
Visualising Trends and Bottlenecks: A Python Web App for QC Progress Monitoring
Paper DV09
PHUSE2025Drug Development
Mapping OMAP Data to SDTM – Use Case for RWD in CAR-T Registry Studies
Paper RE01
PHUSE2025Drug Development
Considerations for the Submission of RWD Using CDISC, with Insights from HL7 FHIR and OMOP
Paper RE02
PHUSE2025Drug Development
Using the USDM and Ensuring Governance and Traceability to Unlock the Potential of Real-World Data Sources for Regulatory Submissions
Paper RE03
PHUSE2025Drug Development
A Customised Algorithm to Evaluate the Quality and Reliability of Real-World Lab Data
Paper RE04
PHUSE2025Drug Development
Real-World Data – Analysis-Ready Datasets: A Standardised, Specialised and Innovative Data Solution for Efficient Real-World Data Analysis
Paper RE05
PHUSE2025Drug Development
Applications of Machine Learning and Artificial Intelligence in Real-World Data in Personalised Medicine for Non-Small Cell Lung Cancer Patients
Paper RE06
PHUSE2025Drug Development
Verifiable Compute to Trust AI in Regulated Workflows
Paper RE07
PHUSE2025Drug Development
Wearable Technology: Enhancing Patient Monitoring and Real-World Evidence
Paper RE08
PHUSE2025Drug Development
From Roadblocks to Roadmaps: Overcoming Challenges in Registry Data Reporting
Paper RE09
PHUSE2025Industry Standards
CDISC 360i: Implementing the CDISC Vision and Roadmap to Connect Standards from Design to Analysis Driving End-to-End Automation
Paper DS01
PHUSE2025Industry Standards
The Development of the CDISC eTFL Portal To Support the Adoption and Implementation of the Analysis Result Standard
Paper DS02
PHUSE2025Industry Standards
CDISC Open Rules: A Deep Dive into Custom Rule Creation
Paper DS03
PHUSE2025Industry Standards
Biomedical Concepts: What Are They and Why Should I Care?
Paper DS04
PHUSE2025Industry Standards
Enable and Automate: A Technical Roadmap Defining CDISC’s Path to End-to-End Automation
Paper DS05
PHUSE2025Industry Standards
Navigating the Complexities of AESI: A Centralised Approach to Molecule-Level Management
Paper DS06
PHUSE2025Industry Standards
Competing on Products, Collaborating on Standards: An Approach to Harmonising Vaccine Regulatory Submissions
Paper DS07
PHUSE2025Industry Standards
End-to-End Therapeutic Area Data Standards Development and Governance – A Case Study Involving CRS and ICANS
Paper DS08
PHUSE2025Industry Standards
Selecting GeARS: Analysis Results Standard Implementation Options for Accelerated Analysis and TFL Automation
Paper DS09
PHUSE2025Industry Standards
Your SCE is Only as Good as Your Data: The Central Role of Information Governance in Clinical Research
Paper DS10
PHUSE2025Industry Standards
Evolution of Genomic Data Mapping from PF to GF in SDTM v3.4: Concepts, Challenges and Controlled Terminology with Genetic Variation Examples
Paper DS11
PHUSE2025Industry Standards
Challenges of Genomic Data in Clinical Trials
Paper DS12