Boosting SAS Programming Efficiency with ChatGPT: A Clinical Trial Perspective
Source category: Connected Health & Machine Learning
Author collections: Illia Skliar
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Clinical Programming Papers and PresentationsPage 22
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 421–440
Building a Large-Scale Clinical Trial’s IT System with In-House Software and OpenClinica
Source category: Application Development
Building an Integrated Preclinical and Clinical Data Platform to Enable Rapid Translational Data Review
Source category: Real-world Evidence
Author collections: Ali Dootson
Building an Internal R Package for Statistical Analysis and Reporting in Clinical Trials: A SAS User’s Perspective
Source category: Solution Development
Author collections: Huei-Ling Chen · Heng Zhou · Nan Xiao
Change is Inevitable: Strategies for Embracing the Industry Shift from SAS-Only to Open Source for Clinical Programmers
Source category: Open Source Technologies
Author collections: Amanda Lopuski
Clinical Graphs Using R
Source category: Poster Presentations
Author collections: Duong Tran
Common Sample Size Calculations for Phase I/IIa Clinical Trials
Source category: Analytics, Big Data & Statistics
Author collections: Aayush Bhoraskar
Confirmation of Best Overall Tumor Response in Oncology Clinical Trials per RECIST 1.1
Source category: Quick Programming Tips
Cybernated Validation of Clinical Reports (TLs)
Source category: Software Demonstrations
Author collections: Giri Balasubramanian · Gopinath Viswanathan
Dashboarding a Clinical Trial Study
Source category: Software Demonstrations
Author collections: Pritesh Desai
Data Doesn’t Lie – Real Time Monitoring and Projecting on Clinical Trial Enrollment Progression
Source category: e-Posters
Author collections: Wenjun He
Data Profiling Made Shiny – Accelerating Clinical Study Delivery and Submission
Source category: Poster Presentations
Decentralized Clinical Data Management (D-CDM): An Innovative 3-Way Approach (Risk-Data-Analytics) to Protect Data Integrity
Source category: Risk-based Monitoring
Author collections: Mukesh Babu K
Detroit, Michigan: A Case Study for DEI Via Decentralised Clinical Trials (DCTs)
Source category: Submissions & Agencies
Author collections: Mark Rothe
Digging Deep into Digital Biomarkers: Empowering Clinical Trials
Source category: Beyond Submissions Stories
Author collections: Vijay Pasapula
Empowering Paediatric Drug Development: CDISC Standards and ICH Guidelines for Clinical Trials with Little Participants
Source category: Data Standards & Governance
Fishing for Code Plagiarism in Clinical SAS Programming
Source category: Scripts & Snippets
Author collections: Menaga Guruswamy Ponnupandy
For Clinical Trials: A Faster and Smoother Approach to Create your SDTM and ADAM Define Specifications for Define.xml with SAS®
Source category: Industry Applications
From Molecules to Effects: Exploring Pharmacokinetics with a Clinical Pharmacology Data Scientist
Source category: Poster Presentations
Generating Clinical Graphs in SAS and R – A Comparison of the Two Languages
Source category: Hands-On Training
Author collections: Kriss Harris · Endri Elnadav