Revolutionise Clinical Trial Data Exploration with {teal}
Source category: Data Visualisation
Author collections: Dony Unardi · Chendi Liao
THE COMMUNITY ARCHIVE
Clinical Programming Papers and PresentationsPage 20
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 381–400
Risk-Based Monitoring Using AI/ML Detection of Systematic Bias in Clinical Data
Source category: Innovation Challenge
Author collections: Kostiantyn Drach · Sergey Glushakov
Semi-Automated and Modularized Approach to Generate Tables for Clinical Study – Categorical Data Report
Source category: Solution Development
Author collections: William Wei · Shunbing Zhao
Serverless Shiny – Evolving Landscape of Clinical Analytics
Source category: Analytics & Statistics
Author collections: Philip Bowsher
Shift gears with ‘gt’: Finely tuned clinical reporting in R using “gt” and “gt summary” packages
Source category: Solution Development
Author collections: Rajprakash Chennamaneni · Sudhir Kedare · Jagan Mohan Achi
SLURM + Open-Source Clinical Workflows: Current State
Source category: Trends & Technology
Author collections: Philip Bowsher · Michael Mayer
Spline Analysis to Understand the Non-linear Relationship in Clinical Research
Source category: Analytics & Statistics
Submitting Patient-Reported Outcome Data in Cancer Clinical Trials- Guidance for Industry Technical Specifications Document
Source category: Submission Standards
Teal as an Open-Source Tool Accelerates Clinical Trial Data Research at GSK
Source category: Open Source Technologies
Teal.builder: A Multifaceted Teal App Builder for Clinical Data Exploration and Reporting
Source category: Emerging Trends
Author collections: Freeman Wang · Andre Couturier
The Prentice-Wilcoxon Test to Study Time to Healing for Split Face, Double Blind, Dermatology Clinical Trials
Source category: Analytics & Statistics
Author collections: Shrutimita Pokhariyal
The Role of the Blinded Programmer in Preparation of Data Monitoring Committee Packages (for Clinical Trials)
Source category: Strategic Implementation & Innovation
Author collections: Binal Mehta · Patel Mukesh
The Significance of Generic Data Transfer Specification for Non-CRF Data in Clinical Trials
Source category: Data Standards & Governance
Author collections: Kristina Zweier
The State of Open-Source Technology in Clinical Data Analysis, Reporting and Submissions – A PHUSE Manuscript
Source category: Open Source Technologies
Author collections: Michael Rimler
Training Domain Specific AI for Clinical Data: Developing an AI Agent to Transform EDC data to CDISC SDTM and then to ADaM Standards
Source category: Lectures
TransCelerate’s Privacy Methodology for Cross-Industry Clinical Data Reuse
Source category: Analytics & Statistics
Author collections: Patty Hegarty
Transcriptomics – A Demanding Data Analysis that Expands the Limits of Regulated Clinical Data Handling
Source category: Data Handling & Engineering
Upholding Blinding in Clinical Trials: Strategies and Considerations for Minimizing Bias
Source category: e-Posters
Usage of OMOP-CDM along with CDISC in Clinical Trials: Challenges and Opportunities
Source category: Real-world Evidence
Author collections: Parag Shiralkar
Using Git and GitLab to Empower QC Workflow and Project Management in Clinical Reporting
Source category: Trends & Technology
Author collections: Kieran Martin