PHUSE2019Programming Languages
Validating R Functions Against SAS Outputs: How RTest Can Build a Bridge Allowing for Validation of R
Paper CT10
Community reference directory
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.
Official links only—files are not hosted by ClinStandards.
Showing 2876–2900 of 4,481 papers
Open official paper
PHUSE2019Programming Languages
Using the Source Code Control System GitHub to Manage Your SAS Code
Paper CT11
PHUSE2019Programming Languages
Understanding Regular Expression and its Application in SAS Using PRX (Perl regEx) Functions
Paper CT12
PHUSE2019Programming Languages
Next Generation Collaboration: Using Tasks and Snippets in SAS Studio
Paper CT13
PHUSE2019Programming Languages
Big SAS Code Navigation and Management
Paper CT14
PHUSE2019Programming Languages
Implementing Imputation Rules and Creating Analysis Flags Following CDISC Guidelines
Paper CT15
PHUSE2019Programming Languages
A Macro Tool to Reduce the Size of the Regulatory Submission Dataset
Paper CT16
PHUSE2019Programming Languages
R or Python? Dilemma, Dilemma…
Paper SM01
PHUSE2019Programming Languages
Validate the Validated: A Python Tool for Study Leads to Review Clinical Outputs
Paper SM02
PHUSE2019Programming Languages
How to Use VBA for CRT: Automating the P21 Community Master Spec
Paper SM03
PHUSE2019Programming Languages
SAS Macro Quoting – A Look Behind the Scenes
Paper SM04
PHUSE2019Programming Languages
An Efficient Way to Combine RTF Files and Create Multi-level Bookmarks and a Hyperlinked TOC
Paper SM05
PHUSE2019Programming Languages
Adapting the SAS Enterprise Guide Log Summary to Check Your LOG for You
Paper SM06
PHUSE2019Programming Languages
Automating Validation of Statistical Reports – A Real Case Study
Paper SM07
PHUSE2019Regulatory Environment
Development of the Standard BIMO Process to Create the Clinsite Dataset
Paper SA01
PHUSE2019Regulatory Environment
Lessons Learned from an FDA Real- time Oncology Review Pilot Programme: A Novartis & Roche Perspective
Paper SA02
PHUSE2019Regulatory Environment
ADaM Submission – How to Work with the Inconsistencies Between the FDA and PMDA Requirements
Paper SA03
PHUSE2019Regulatory Environment
Processing Big Data from Multiple Sources
Paper SA04
PHUSE2019Regulatory Environment
How Metadata Can Help Drive the Creation of Tables, Figures and Listings
Paper SA05
PHUSE2019Regulatory Environment
Developing SEND for CBER – Collaborative Workstream Initiative
Paper SA06
PHUSE2019Regulatory Environment
Navigating FDA Requirements: ISS/ISE Build Strategies
Paper SA07
PHUSE2019Regulatory Environment
Identifying Hurdles for Submission of Electronic Nonclinical Data (SEND)
Paper SA08
PHUSE2019Regulatory Environment
Impact of SEND Data on FDA Review of Nonclinical Studies
Paper SA09
PHUSE2019Regulatory Environment
Using CDISC-SEND Standardized Data in FDA Toxicology Review: The KickStart Service
Paper SA10
PHUSE2019Regulatory Environment
The Clinical Data Specialist Role Within Regulatory Review
Paper SA13