The Use of Meta Data in Creating, Transforming and Transporting Clinical Data
Source category: CDISC and Industry Standards
Author collections: Gregory Steffens
THE COMMUNITY ARCHIVE
Clinical Programming Papers and PresentationsPage 57
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.
1,393 papers · Showing 1121–1140
Uncover Useful Patterns in Clinical Trials Safety Data with JMP® Clinical
Source category: Technical Solutions
Author collections: Valerie Nedbal
Useful Tips for Analysis of Variance (ANOVA) in Multicentre, Placebo Controlled Clinical Trials
Source category: Statistics and Pharmacokinetics
A Framework for Acheiving an Industry-Driven, Open-Source Clinical Reporting System
Source category: Posters
Author collections: Dante DiTommaso · Ann Martin
Accelerate Clinical Development through Management of Data Quality
Source category: Data Handling
Author collections: David Smith
BRIDGing CDASH to SAS: How Harmonizing Clinical Trial and Healthcare Standards May Impact SAS Users
Source category: CDISC Methodologies for FDA Submissions
Building and maintaining a clinical data warehouse - challenges and opportunities for pharmaceutical programmers
Source category: Management
Clinical Database acceptance: what statistical review checks are necessary to validate a database?
Source category: Data Handling
Clinical DI Studio - will we need new MetaProgrammers?
Source category: Applications and Software Development
Clinical SAS® Programming: Analysis and Mitigation of Risk
Source category: Pharma, Life Sciences and Healthcare
Author collections: Parag Shiralkar
Clinical Trial Reporting Using SAS/GRAPH� SG Procedures
Source category: Pharma, Life Sciences and Healthcare
Author collections: Susan L. Schwartz
Clinical Trial Reporting with SAS ODS Graphics
Source category: Technical Solutions
Author collections: David Garbutt
ClinicalTrials.gov- a programmers perspective
Source category: Regulatory
Author collections: Ralf Minkenberg
Does a Sponsor Clinical Trial Reporting System Fit Into a Sponsor/CRO Alliance?
Source category: Management
ETL and the Clinical Programmer – They don’t have to be Enemies!
Source category: Data Handling
Author collections: Chris Decker · Chris Olinger
Graphics of Clinical Data: A Picture is Worth a Thousand Tables
Source category: Tutorials
Publisher slides file PRE_TS03.pdf returned HTTP 403 on 17 October 2026.
Industry Standard Good Programming Practice for Clinical Trials (using SAS)
Source category: Regulatory
Author collections: Mark Foxwell
Retirement of Legacy Clinical Systems and Moving to SAS® Drug Development, Much More than Just Moving the Data
Source category: Systems Architecture
Author collections: Fred Forst
Software validation in clinical trials: strategy, implementation and experiences in the MAKS project
Source category: Posters
Standardization of data base: interaction between Biostatistics and Clinical Data Management
Source category: CDISC and Industry Standards
Author collections: Celine Tendero