PHUSE2023·Connect·Programming LanguagesSAS Macro for Converting Variable Attributes from XLSX Specifications to SDTM/ADAM SAS data sets SS03 US · FloridaSee metadata
PHUSE2023·Connect·Programming LanguagesUp-to-Date with Dates – Imputation Rules in R Compared to SAS SS05 US · FloridaSee metadata
PHUSE2023·Connect·Programming LanguagesHow Python or R Support/Facilitate the Validation Process of TFLs for a Study Development Using Hybrid SAS and R SS06 US · FloridaSee metadata
PHUSE2023·Connect·Programming LanguagesExploring the Possibility of Automating SDTM Domain Subject Visits (SV) SS08 US · FloridaSee metadata
PHUSE2023·Connect·Regulatory EnvironmentDrafting Your Plain Language Summaries: Hurdles to Overcome and How to Overcome Them SA01 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentInvestigator Initiated Trials: Turbulence ahead! SA01 US · FloridaSee metadata
PHUSE2023·Connect·Regulatory EnvironmentRegulating the Future: Navigating the Complexities of 3D Printing in the Pharmaceutical Industry SA02 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentDetroit, Michigan: A Case Study for DEI Via Decentralised Clinical Trials (DCTs) SA03 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentWorking Together: The Evolving Relationship of Biostatistics & Regulatory for Support of Study Data Standardization Plans and BIMO Reviewer's Guides SA03 US · FloridaSee metadata
PHUSE2023·Connect·Regulatory EnvironmentSubmission Experience with Real-Time Oncology Review, Project Orbis, and Priority Review SA04 US · FloridaSee metadata
PHUSE2023·Connect·Regulatory EnvironmentFDA Dataset Walkthrough - Statistical Programming Perspectives SA05 US · FloridaSee metadata
PHUSE2023·Connect·Regulatory EnvironmentPractical Operations of Electronic Study Data Submissions SA05 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentDevelopment Safety Update Report (DSUR)/Periodic Safety Update Report (PSUR) SA07 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentInteraction with the FDA During and After a Type C Meeting, From the Perspective of a Statistical Programmer SA08 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentIt’s Easy Peasy Submitting Data to the China NMPA – Really? SA10 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentUnleashing the Role of a Statistical Programmer in Expediting a Submission, Novartis SA12 EU · BirminghamSee metadata
PHUSE2023·Connect·Regulatory EnvironmentUse Python to Make Clinical Trial Result Posting Automatically ST07 US · FloridaSee metadata