A Methodology of Laboratory Data Reporting of Potentially Clinical Significant Abnormality (PCSA) for Clinical Study Report
Source category: Beyond the Basics
Author collections: Xiangchen (Bob) Cui · Min Chen
THE COMMUNITY ARCHIVE
Clinical Programming Papers and PresentationsPage 47
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 921–940
A New Era: Open access to clinical Trial Data – A case study
Source category: Beyond the Basics
Author collections: Aruna Kumari Panchumarthi · Jacques Lanoue
A Way to Manage Clinical Project Metadata in SAS® Enterprise Guide
Source category: Applications Development
AstraZeneca Clinical Trial Transparency and External Sharing of Individual Patient-level Data
Source category: Poster Presentations
Automating Clinical Trial Reports with ODS ExcelXP Tagset
Source category: Quick Tips
Author collections: John O’Leary
Begin with the End in Mind – Using FDA Guidance Documents as Guideposts when Planning, Delivering and Archiving Clinical Trials
Source category: Submission Standards
Author collections: David C. Izard
Clinical Data to Information: Quick, Standardised and Validated with Knowledge of PROC FCMP
Source category: Technical Solutions
Author collections: Cathal Gallagher
Clinical knowledge helps SAS programmers in the pharmaceutical industry get job done better
Source category: Career Planning
Author collections: YINGQIU YVETTE LIU
CodEX - When Excel Meets SAS to Code Clinical Data
Source category: Data Handling
Author collections: Stephane Chollet · Cathy Scoupe
Concept and Implementation of an Efficient Version Control System for SAS® Programs in Clinical Development
Source category: Technical Solutions
Author collections: Dirk Spruck
CRO, TLF, SOP? OMG!: A Beginner’s Guide to the Clinical Research Organization
Source category: Career Planning
Data-centric System Development Life Cycle for Automated Clinical Data Development Systems
Source category: Applications and Software Development
Author collections: Kevin Lee
De-Id: 'The What' and 'The How' of de-identifying your Clinical Trial Data
Source category: Software Demonstrations
Author collections: Gavin Winpenny · Stephen Bamford
Development of a Clinical SAS University Training Program in Eastern Europe
Source category: Management and Support
Author collections: Sergey Glushakov
Driving Quality into Clinical Trials
Source category: Software Demonstrations
Author collections: Erik Doffagne
Efficient Data Reviews and Quality in Clinical Trials Using CDISC Data Standards
Source category: Software Demonstrations
Firefighters – clinical trial analysis teams
Source category: Management and Support
Author collections: Iryna Kotenko
Graphical Presentation of Clinical Data in Oncology Trials
Source category: Data Visualization and Graphics
Author collections: Murali Kanakenahalli · Avani Kaja
Hands-on Data Mining, Digging up clinicaltrials.gov Data with SAS 9
Source category: Coding Solutions
Author collections: Mahdi About
How a Clinical Data Repository can Support Pharmacovigilance
Source category: Data Handling
Author collections: Pantaleo Nacci