Official-source directory
Conference Papers
13,885
available papers
10
available conferences
Papers
Showing 1341–1360 of 3,683
PHUSE2023·Connect·Programming Languages
Exploring the Possibility of Automating SDTM Domain Subject Visits (SV) SS08 US · Florida
PHUSE2023·Connect·Regulatory Environment
Drafting Your Plain Language Summaries: Hurdles to Overcome and How to Overcome Them SA01 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
Investigator Initiated Trials: Turbulence ahead! SA01 US · Florida
PHUSE2023·Connect·Regulatory Environment
Regulating the Future: Navigating the Complexities of 3D Printing in the Pharmaceutical Industry SA02 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
Detroit, Michigan: A Case Study for DEI Via Decentralised Clinical Trials (DCTs) SA03 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
Working Together: The Evolving Relationship of Biostatistics & Regulatory for Support of Study Data Standardization Plans and BIMO Reviewer's Guides SA03 US · Florida
PHUSE2023·Connect·Regulatory Environment
Submission Experience with Real-Time Oncology Review, Project Orbis, and Priority Review SA04 US · Florida
PHUSE2023·Connect·Regulatory Environment
Practical Operations of Electronic Study Data Submissions SA05 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
FDA Dataset Walkthrough - Statistical Programming Perspectives SA05 US · Florida
PHUSE2023·Connect·Regulatory Environment
Development Safety Update Report (DSUR)/Periodic Safety Update Report (PSUR) SA07 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
Interaction with the FDA During and After a Type C Meeting, From the Perspective of a Statistical Programmer SA08 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
It’s Easy Peasy Submitting Data to the China NMPA – Really? SA10 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
Unleashing the Role of a Statistical Programmer in Expediting a Submission, Novartis SA12 EU · Birmingham
PHUSE2023·Connect·Regulatory Environment
Use Python to Make Clinical Trial Result Posting Automatically ST07 US · Florida
PHUSE2023·Connect·Regulatory Environment
Innovate Clinical Trial Reporting with Open Source ST08 US · Florida
PHUSE2023·Connect·Regulatory Environment
Handling Multiple Adaptations in One Clinical Trial ST09 US · Florida
PHUSE2023·Connect·Regulatory Environment
Digging Deep into Digital Biomarkers: Empowering Clinical Trials ST10 US · Florida
PHUSE2023·Connect·Technology & Applications
H2H Portal – A Shiny Automation of Reproducible and Traceable Analysis and Reporting Using a Metadata Framework AD01 EU · Birmingham