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14 papers and 1 presentation; 14 titles.

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Conference ×	Year ×	Title ×	Authors	Extras	Pages
PharmaSUG	2026	Creating Reproducible Clinical Output with SASSY - Reporter Package	Vicky Yuan	source	16
PHUSE US	2025	Navigating the Complexities of AESI: A Centralised Approach to Molecule-Level Management	Tian Fang, Xiaojing Zhu	source presentation source	7
PHUSE US	2023	Connecting Tables, Listings and Figures [presentation]	Stella Guo	source video	11
PHUSE US	2020	Volcano Plot: Demystifying Why and How	Chandana Sudini, Jyothi Nelakurthi	source presentation source	9
PHUSE US	2018	Drug-Induced Liver Injury (DILI) Classification Using FDA-Approved Drug Labeling and FAERS Data - FDA	Qais Hatim	source presentation source	31
PharmaSUG	2014	Common and Comparative Incidence Indicators of Adverse Events for Well-Defined Study Pools	John R. Gerlach	source	7
PHUSE EU	2008	Statistically guided review of safety data in clinical trials	Michael O'Connell, Harry Southworth	source	12
PharmaSUG	2008	Labor-Saving SQL Constructs	Brian P. Fairfield-Carter, David W. Carr		11
SGF	2008	Labor-Saving SQL Constructs	Brian P. Fairfield-Carter, David W. Carr	source	10
PHUSE EU	2007	Bayesian Modelling with SPLUS and the S+flex Bayes library	Andrew Jack, Dawn Woodard	source	11
PharmaSUG	2007	Can Coding MedDRA and WHO Drug Be as Easy as a Google Search?	Sy J. Truong		9
SGF	2007	Can Coding MedDRA and WHO Drug Be as Easy as a Google Search?	Sy J. Li, Na Truong	source	9
PharmaSUG	1998	SAS Techniques for Developing an Intranet Drug Safety Review System	Dennis X. Tang, Mickey Cheng		10
PharmaSUG	1997	Adverse Events Summary Tables in Clinical Trials: Incorporating P-values Using SAS Macros and SAS/AF	Incorporating P-values		10
SEUGI	1990	A SAS Software Based Clinical Trials Data Management System Used at Hoffmann-La Roche	Mark Aellen-Rumo, M. Rainisio	source	13

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