PharmaSUG2024paper·US·Data Standards
Around the Data DOSE-y Doe, How Much Fun Can Your Data Can Be: Using DOSExx Variables within ADaM Datasets DS-193
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PharmaSUG2024paper·US·Data Standards
A New Way to Automate Data Validation with Pinnacle 21 Enterprise CLI in LSAF DS-205
PharmaSUG2024paper·US·Data Standards
Programming Considerations in Deriving Progression-Free Survival on Next-Line Therapy (PFS2) DS-271
PharmaSUG2024paper·US·Data Standards
I Want to Break Free: CRF Standardization Unleashing Automation DS-280
PharmaSUG2024paper·US·Data Standards
ADaM Design for Prostate Cancer Efficacy Endpoints Based on PCWG3 DS-287
PharmaSUG2024paper·US·Data Standards
Guideline for Creating Unique Subject Identifier in Pooled studies for SDTM DS-305
PharmaSUG2024paper·US·Data Standards
CDISC Therapeutic Area User Guides and ADaM Standards Guidance DS-342
PharmaSUG2024paper·US·Data Standards
Protocol Amendments and EDC Updates: Downstream impact on Clinical Trial Data DS-353
PharmaSUG2024paper·US·Data Standards
A quick guide to SDTM and ADaM mapping of liquid Oncology Endpoints. DS-360
PharmaSUG2024paper·US·Data Standards
Handling of Humoral and Cellular Immunogenicity Data in SDTM DS-367
PharmaSUG2024paper·US·Data Standards
Implementation of composite estimands for responder analysis based on change from baseline in non-solid tumours DS-374
PharmaSUG2024paper·US·Data Standards
Streamlining Patient-reported outcome (PRO) data standardization & analysis DS-398
PharmaSUG2024paper·US·Data Standards
AI and the Clinical Trial Validation Process – Paving a Rocky Road DS-400
PharmaSUG2024paper·US·Data Standards
Game changer! The new CDISC ADaM domain ADNCA for PK/PD data analysis DS-406
PharmaSUG2024paper·China·Data Standards and Submission (DS)
Extracting Useful Information from XFDF Format of aCRF Annotations DS-10024 Beijing