PHUSE2020Programming Languages
PROC FCMP or Function You Create, Master and Proceed
Paper SM08
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Conference Papers
Find papers in official PHUSE, PharmaSUG, and WUSS proceedings. Search by title or paper number, then narrow the directory by conference, year, or category.
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Showing 2676–2700 of 4,481 papers
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PHUSE2020Regulatory Environment
Real-time Oncology Review – Applicant Experience
Paper SA01
PHUSE2020Regulatory Environment
The Misery of the Miscellaneous Folder in Module 5
Paper SA02
PHUSE2020Regulatory Environment
Data Standards Used for Electronic Submission of Real-world Evidence in New Drug Applications (NDAs)
Paper SA03
PHUSE2020Regulatory Environment
FDA Study Data Guidance Update
Paper SA04
PHUSE2020Regulatory Environment
Getting It Right: Refinement of SEND Validation Rules
Paper SA05
PHUSE2020Regulatory Environment
A Case Study: Data Transparency of Clinical Trial Data
Paper SA06
PHUSE2020Regulatory Environment
Regulatory Scrutiny on Data Integrity: Are You Safe?
Paper SA07
PHUSE2020Regulatory Environment
An Update on CDISC-SEND Data Submissions to the FDA
Paper SA08
PHUSE2020Regulatory Environment
The JumpStart Traceability Assessment
Paper SA09
PHUSE2020Regulatory Environment
Developing SEND for CBER – Collaborative Workstream Initiative Update
Paper SA10
PHUSE2020Regulatory Environment
Programmatic Generation of Health Canada's Comparative Bioavailability Information Appendix B
Paper SA11
PHUSE2020Regulatory Environment
Managing Simultaneous Drug Submissions with Breakthrough Designations – Lessons Learned from a Programming Perspective
Paper SA12
PHUSE2020Regulatory Environment
Getting Closer to Multi-regional Clinical Trials
Paper SA13
PHUSE2020Regulatory Environment
Industry Experiences Submitting Standardized Study Data to Regulatory Authorities
Paper SA14
PHUSE2020Technology & Applications
Breaking Boundaries: Working Across Different Workspaces in LSAF
Paper AD09
PHUSE2020Technology & Applications
R Shiny for Exploratory Analysis of Phase III Trial Results
Paper AD16
PHUSE2020Technology & Applications
SPA – A Catalyst for Clinical Protocol Development
Paper SD02
PHUSE2020Technology & Applications
CDISC Library Try-out: From Implementation to Evaluation of the API
Paper SD05
PHUSE2020Technology & Applications
Regulatory Report Automation with R
Paper SD09
PHUSE2020Technology & Applications
Analysis Studio: A Tool Framework for Supporting Regulatory Review
Paper SD10
PHUSE2020Technology & Applications
Quarterly Safety Reporting: Timely Analysis of Clinical Safety Data Using Qlik Sense Software
Paper SD11
PHUSE2020Technology & Applications
Big Data Analytics with JuliaDB
Paper SD12
PHUSE2020Technology & Applications
Life Science's Process Automation of Systems and Solutions
Paper SD14
PHUSE2020Technology & Applications
Using Graph Technology for Metadata-driven Clinical Development
Paper TT01