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system organ class

77 papers and 14 presentations; 86 titles.

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Conference × Year × Title × Authors Extras Pages
PharmaSUG CN 2026 From SAP to TFL: An AI-Assisted Workflow Framework for Automated Shells and TFLs Xiaoyu Ding,
Guoqing Zhao,
Huafeng Gao,
Zhiyuan Guo		 source 18
PharmaSUG CN 2026 The reporter package: A Powerful Reporting Package to Replicate SAS Output Bill Huang source 24
PharmaSUG 2026 Interactive Safety Data Visualization Platform: Transforming Adverse Event Analysis Review Through Dynamic Dashboards in Clinical Trials Nishanth Chinthala,
Alexandr Hromcenco		 source 5
PHUSE US 2026 Comparing Medical Queries with Interactive Graphics using JMP Clinical Chris Kirchberg source
presentation source		 7
PHUSE US 2026 Open Source Pavilion: Metadata-driven Automation Interactive [presentation] Orla Doyle,
Rammprasad Ganapathy		 source 28
PharmaSUG 2025 Clopper Pearson CI? get your data ready for it! Ruth Marisol Rivera Barragan,
Isaac Vazquez		 source 7
PharmaSUG 2025 Hands-on Training: eTFL Portal & TFL Designer Community Bhavin Busa source 8
PHUSE US 2025 Enhancing Clinical Trial Data Queries with LLMs and Neo4j: A Flexible Framework for ADaM Dataset Management Jaime Yan source
presentation source		 28
PHUSE US 2025 Selecting GeARS: Analysis Results Standard Implementation Options for Accelerated Analysis and TFL Automation Bhavin Busa,
Richard Marshall		 source
presentation source		 10
PHUSE US 2025 The Development of the CDISC eTFL Portal To Support the Adoption and Implementation of the Analysis Result Standard Bess LeRoy,
Bhavin Busa		 source
presentation source		 8
PHUSE EU 2024 Interactive reporting using FDA Standard Safety Shells and CDISC Analysis Results Standard Megan Harries source
presentation source		 5
PHUSE EU 2024 The Development of the CDISC eTFL Portal to Support the Adoption and Implementation of the Analysis Results Standard Bess LeRoy,
Bhavin Busa		 source
presentation source		 8
SESUG 2024 Efficient Way to Create Adverse Event (AE) Summary Tables by System Organ Class (SOC) and Preferred Term (PT) using PROC SQL in SAS Hardik Sheth source 8
PharmaSUG 2024 Comparing SAS and R Approaches in Creating Multicell Dot Plots in Statistical Programming Yi Guo source 14
PharmaSUG 2024 Creating Adverse Event Tables using R and SASSY System Vicky Yuan source 11
PharmaSUG 2024 Demystifying Incidence Rates: A Step-by-Step Guide to Adverse Event Analysis for Novice Programmers Yuting Peng,
Ruohan Wang		 source 10
PharmaSUG 2024 Pictorial Representation of Adverse Events (AE) Summary - A new perspective to look at the AE data in Clinical Trials Pradeep Acharya,
Anurag Srivastav		 source 11
PHUSE US 2024 USUBJID Challenges: Representing Multiple Participations for Analysis and Reporting Emily Bernstein-Hanlon,
Sirisha Davuluri		 source
presentation source		 9
PHUSE EU 2023 Building an integrated pre-clinical and clinical data platform to enable rapid translational data review Brenda Finney,
Ali Dootson Instem		 source
presentation source		 12
WUSS 2023 Generation of AE (Adverse Events) summary tables by worst CTC Grade utilizing SAS Ballari Sen source 14
PharmaSUG 2023 Introducing TFL Designer: Community Solution to Automate Development of Mock-up Shells and Analysis Results Metadata [presentation] Bhavin Busa,
Navin Dedhia		 source 13
PHUSE US 2023 Friends Don't Let Friends Make Ugly Dashboards [presentation] Marcia Powers,
Deidre Kreifels		 source
video		 14
PHUSE EU 2022 Best Practices for Automated Delivery Set-up, from Raw Data to CRT, with Methods to Standardise and Streamline Programming and Delivery Processes [presentation] Daniel Carden source
video		 21
WUSS 2022 Child Data Set: An Alternative Approach for Analysis of Occurrence and Occurrence of Special Interest Lindsey Xie,
Richann J. Watson,
Jinlin Wang,
Lauren Xiao		 source 15
PharmaSUG 2022 ADaM Child Data Set: An Alternative Approach for Analysis of Occurrence and Occurrence of Special Interest Lindsey Xie,
Richann J. Watson,
Jinlin Wang,
Lauren Xiao		 source 15
PHUSE US 2022 'Verify Outputs' Product Demonstration: Validation of Statistical Outputs Using Automation [presentation] Ilan Carmeli,
Yoran Bar		 source
video		 17
PHUSE US 2022 Real-time Interactive Dashboard for Clinical Trials [presentation] Kris Liu source 9
PHUSE EU 2021 Visualising Knowledge Graphs: Information Solution or Ball of Confusion? [presentation] Tim P. Williams source
video		 57
PHUSE US 2021 Do EudraCT the Easy Way: Semi-automation of Inputting Study & Treatment Event Information in EudraCT [presentation] Kevin Miller,
Larry Sleeper		 source
video		 21
PHUSE US 2021 Dynamic Macro Using the Convergence Dataset to Generate the Odds Ratio (OR), Risk Ratio (RR) and Risk Difference (RD) per SOC and PT Using the Genmod Procedure [presentation] Jagadish Katam source
video		 26
PHUSE US 2021 FDA & PMDA Validator Rules - What, Why and How ... But Should You Care? [presentation] Charanjit Kahlon,
Kishore Pothuri		 source
video		 21
PHUSE US 2021 Indenting Lengthy Text Strings in PROC REPORT Outputs [presentation] Jeppe Juul,
Kavita Math		 source
video		 19
PharmaSUG 2021 Graphical Representation of Clinical Data using Heat Map Graph Pavani Potuganti,
Sree Nalluri		 source 10
PharmaSUG 2021 Macro Development from Design to Implementation Applied to Occurrence Data Frequency Analysis Chengxin Li,
Michael Pannucci,
Toshio Kimura		 source 9
PHUSE EU 2020 Preparing for FDA and PMDA Submission Simultaneously - What to Leverage, How to Deal with the Differences Efficiently [presentation] Jasmine Kestemont source
video		 22
SESUG 2020 Upgrading Clinical Trial Reports from ODS LISTING to ODS TAGSETS.RTF Christopher J. Smith source 25
SGF 2020 Upgrading Clinical Trial Reports from ODS LISTING to ODS TAGSETS.RTF Christopher J. Smith,
Joshua M. Horstman		 source 25
PharmaSUG 2020 Macro for controlling Page Break options for Summarizing Data using Proc Report Sachin Aggarwal,
Sapan Shah		 source 7
PHUSE US 2020 Interactive Adverse Event Data Visualization Using R Shiny Aditya Rachoori,
Mukul K Mittal		 source 9
WUSS 2019 Bespoke outputs, just like everyone else's: using the SAS Macro Language to create template programs for standard presentations of your client's clinical trial data Sean-Paul A. Claypool source 9
PHUSE US 2019 Adverse Events of Special Interest (AESI) Tabulation Chuanfeng Shih source
presentation source		 5
SESUG 2017 A Macro for Generating the Adverse Events Summary for ClinicalTrials.gov Andrew Moseby,
Maya Barton		 source 7
MWSUG 2017 Patient Safety with SAS Visual Analytics Piyush K. Singh,
Prasoon Sangwan,
Ghiyasuddin Mohammed Faraz Khan		 12
PharmaSUG 2017 Innovation and Regulatory Review What is JumpStart? Alan Shapiro source 24
WUSS 2016 Indenting with Style Bill Coar source 7
PharmaSUG 2016 AE: An Essential Part of Safety Summary Table Creation Rucha Landge source 12
PharmaSUG 2016 SAS Macro for Summarizing Adverse Events Julius Kirui,
Rakesh Mucha		 source 11
SESUG 2015 Reporting of treatment emergent adverse events based on pooled data Analysis or Country Specific Submissions: A case study Sheetal Shiralkar source 8
PharmaSUG CN 2015 Hands-On ADaM ADAE Development Sandra Minjoe 7
PharmaSUG 2015 A Practical Approach to Create Adverse Event Summary by Toxicity Grade Table Zhengxin (Cindy) Yang source 8
PHUSE EU 2014 Exploring Safety and Diagnostic Data using Self-Organising Maps Colin de Klerk source
presentation source		 9
PHUSE EU 2014 MedDRA - Beyond that Basic AE Report. How SMQs and MedDRA Structure can Enhance Reporting Pamela J. Giese source
presentation source		 9
PharmaSUG 2014 Common and Comparative Incidence Indicators of Adverse Events for Well-Defined Study Pools John R. Gerlach source 7
PharmaSUG 2014 Hands-On ADaM ADAE Development Sandra Minjoe,
Kimberly Minkalis		 source 7
SESUG 2013 Imputing Dose Levels for Adverse Events John R. Gerlach,
Igor Kolodezh		 source 8
PharmaSUG 2013 Efficient Statistical Review Using the ExcelXP Tagset Bradford J. Danner source 5
PharmaSUG 2013 Everything You Need To Know About Standardised MedDRA Queries Rajkumar Sharma source 6
PharmaSUG 2013 Hands-On ADaM ADAE Development Sandra Minjoe source 7
PharmaSUG 2013 Imputing Dose Levels for Adverse Events John R. Gerlach,
Igor Kolodezh		 source 8
PharmaSUG 2013 MedDRA - Beyond that Basic AE Report. How SMQs and MedDRA Structure can Enhance Reporting Pamela J. Giese source 10
PharmaSUG 2013 The Hash of Hashes as a "Russian Doll" Structure: Application to Clinical Adverse Events Data Analysis Joseph W. Hinson source 12
PharmaSUG 2013 Traceability in the ADaM Standard Ed Lombardi source 8
SGF 2013 Assessing Drug Safety with Bayesian Hierarchical Modeling Using PROC MCMC and JMP Richard C. Zink source 13
SGF 2013 Using the ADaM ADAE Structure for Non-AE Data Mario Widel,
Sandra Minjoe		 source 13
NESUG 2012 Kick It Old School - Creating Reports with the DATA _NULL_ Step Sai Ma,
Suwen Li,
Minlan Li		 10
PharmaSUG 2012 Experience of Generating an XML file and Uploading Serious and Frequent Adverse Events to ClinicalTrials.gov Juan Wu,
Min Lai		 source 9
PharmaSUG 2012 PROGRAMMER'S SAFETY KIT: Important Points to Remember While Programming or Validating Safety Tables Sneha Sarmukadam,
Sandeep Sawant		 source 11
SGF 2012 ODS PDF and RTF Application Development: Steps to Ensure Success and Examples of Useful Coding Techniques Benno F. Kurch source 12
NESUG 2011 A Practical and Efficient Approach in Generating AE (Adverse Events) Reports Within a Clinical Study Environment Jiannan Hu 8
PHUSE EU 2010 GSTARS a complete strategy for the reporting [presentation] Alain Vasseur source 30
SGF 2010 Data Simulation for Piloting Clinical Trials Display Programs Brandon L. Welch,
Rita Slater		 source 9
PHUSE EU 2009 Coding dictionaries information: How to manage? How to use? Guimard Herve,
Eric Sorel		 source
presentation source		 2
PharmaSUG 2009 %ANYTL: A Versatile Table/Listing Macro Yang Chen 11
PharmaSUG 2009 A SAS Macro for Creating Adverse Event Analysis Dataset Daniel Li,
Suwen Li,
Stephanie Sproule		 10
PharmaSUG 2009 A Statistical Analysis System for Categorical Data using SAS Cheng Jun Tian 10
PHUSE EU 2008 Statistically guided review of safety data in clinical trials Michael O'Connell,
Harry Southworth		 source 12
NESUG 2008 Multiple Adverse Event Tables without Surgical Intervention Adel Fahmy,
Carol Matthews		 11
PharmaSUG 2008 Automate Compiling Clinical Appendix Tables and Listings into a Review Package with a Hyper-Linked Table of Contents Xiangchen (Bob) Cui,
Wei Zhang		 20
PharmaSUG 2008 EZTABLE Macros Daniel Huang 12
NESUG 2007 Great Expectations of PROC FORMAT - Applications All You Can Do with Formats in the SAS System John He,
Ram Valluru		 8
PHUSE EU 2007 Bayesian Modelling with SPLUS and the S+flex Bayes library Andrew Jack,
Dawn Woodard		 source 11
PharmaSUG 2007 A Scalable Platform For Clinical Trials - Interoperability And Automation In A Web-Based Environment John R. Gerlach,
Maulik Shah		 11
PharmaSUG 2007 Challenge the Specs Catherine Edwards 7
PharmaSUG 2007 Using the SAS Information Delivery Portal in the Pharmaceutical Sector Raymond Ebben 12
PHUSE EU 2006 Using the SAS Information Delivery Portal in the Pharmaceutical Sector Raymond Ebben source 12
NESUG 2006 Using PROC CDISC Chauthi Nguyen 5
PharmaSUG 2006 Page Breaks: Simple and Effective Ways to Neatly Present Data Suzanne M. Humphreys 9
PHUSE EU 2005 Implementing Shared Column Variables Shan Lee source 8
PharmaSUG 2004 One Frequency Macro for All Frequency Tables Sam Mao 9
SEUGI 1998 Development of an interactive review and reporting tool based on SAS/PH-Clinical software [presentation] Sylvia Pratz source 33
SEUGI 1989 SAS/AF Software In Clinical Data Applications Mark Crawford source 26

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