Impact of Drug Accountability on Drug Compliance and Dose Intensity in Clinical Trials
Source category: Data Standards
Author collections: Vishal Gandhi · Milan Adesara
THE COMMUNITY ARCHIVE
Clinical Programming Papers and PresentationsPage 13
Clinical programming connects study data, standards, analysis and reporting. Explore implementation papers on clinical trials, validation and repeatable workflows, then follow a focused topic for a particular dataset or deliverable.
981 papers · Showing 241–260
Integrating Gen AI with an Open-Source Toolkit for Clinical Insight Generation to Boost Data Science Efficiency
Source category: OS
Author collections: Vincent Shen
Interactive Insights: Leveraging R Shiny for Enhanced Data Visualisation in Clinical Trial Readouts
Source category: Data Visualisation (DV)
Interactive Longitudinal Data Analysis and Visualization in Clinical Research Using R.
Source category: R, Python, and Open Source Technologies
Interactive Visualisation of Pooled Clinical Trial Safety Data
Source category: Emerging Trends
Author collections: Ling Zhang
JazzAIR: Advancing Clinical Study Reporting Through Modern Development Practices and Testing Strategy
Source category: Application Development (AD)
Author collections: Chen Yang
Key Metrics for Success: Measuring Project Performance and Impact in the Face of Complex Clinical Trials
Source category: Professional Development
Author collections: Kavya Yachamaneni · Hayley MacKenzie
Kraken: A Shiny Application for Visualising SDTM Data in Early-Phase Clinical Trials
Source category: Scripts, Macros & Automation
Landmark Analysis: A Method for Accurate Prediction of Time-Dependent Clinical Risks and Their Effect on Patient Outcomes
Source category: Statistics and Analytics
Author collections: Sunil Kumar Pusarla · Avani Alla
Last Observation Carried Forward (LOCF) in Longitudinal Clinical Studies: Adopting a Functional Approach to Imputing Missing Values Using PROC FCMP
Source category: Pharma and Life Sciences
Author collections: Troy Hughes
Last Observation Carried Forward (LOCF) in Longitudinal Clinical Studies: Adopting a Functional Approach to Imputing Missing Values Using PROC FCMP, the SAS® Function Compiler
Source category: Solutions Development
Author collections: Troy Hughes
Last Observation Carried Forward (LOCF) in Longitudinal Pharmaceutical and Clinical Trials Studies: Adopting a Functional Approach to Imputing Missing Values Using PROC FCMP, the SAS Function Compiler
Source category: Data Collection, Management, and Manipulation (DCMM)
File inside source ZIP: 61-Troy-Hughes-supporting-document.pdf
Author collections: Troy Hughes
Leveraging HASH Technologies for Enhanced Clinical Trial Programming Efficiency
Source category: Scripts, Macros & Automation
Leveraging NLP for Clinical Trial Efficiency: Development of a Protocol-Aware AI Chatbot
Source category: Machine Learning, AI and Large Language Models
Leveraging Open-Source Python Tools to Improve Efficiency and Transparency in Clinical Trials
Source category: Open Source Technologies (OS)
Author collections: Sohan Lal
LLMs in Clinical Trials: Overcoming Challenges Related to Patient Confidentiality and Intellectual Property
Source category: Machine Learning, AI and Large Language Models
Author collections: Amit Javkhedkar
Low-Code Solutioning in SAS Viya for Automated Clinical Data Quality, Decisioning and Harmonization
Source category: Solution Development
Author collections: Mary Dolegowski · Scott McClain
Milestones Matter: Understanding Key Milestones in Clinical Trials
Source category: Poster Presentations (PP)
Author collections: Satyapal Gudla
Mind the Gaps: Automating Multiple Imputation in Clinical Trial Workflows
Source category: Pharma and Life Sciences
Author collections: Jiangang Cai
Modernising Clinical Data Science: Best Practices for a Unified, Governed SCE
Source category: Application Development (AD)
Author collections: Matthew Tendler