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113 papers and 21 presentations; 126 titles.

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Conference × Year × Title × Authors Extras Pages
PharmaSUG 2026 Beyond WHODrug: Insight into Concomitant Medication Data Analysis Song Liu,
Martin Nielsen,
Rambabu Sura		 source 9
PharmaSUG 2026 Harmonizing History: A Framework for Deriving Line of Therapy in Complex Integrated Summaries. Bhargav Koduru,
Kavitha Guddam,
Santosh Reddy Lekkala		 source 15
PHUSE US 2026 Balancing Privacy and Utility with Smart Anonymisation [presentation] Zach Weingarden source 13
PHUSE US 2026 Interactive Patient Profiles in R Shiny: Enhancing Narrative Review in Clinical Studies Danny Hsu,
Tzu-Chien Chuang		 source
poster source		 4
PHUSE US 2026 Multiple Sclerosis Trials Unpacked: Standards, Endpoints and Programming Experience Daryna Teteriuk source
presentation source		 12
PHUSE EU 2025 SI Add More MSG to Your Annotations [presentation] Davy Baele,
Nicolas Deravet		 source 19
PharmaSUG 2025 Which ADaM Data Structure Is Most Appropriate? Gray Areas in BDS and OCCDS. Veronica Gonzalez source 15
PHUSE US 2025 Accelerating Patient Safety with Knowledge Graphs: Lessons from a Successful Implementation Partha Bhattacharjee,
Kirti Aggarwal		 source
presentation source		 10
PHUSE US 2025 Considerations for the Submission of RWD using CDISC with Insights from HL7 FHIR and OMOP Ingeborg Holt,
Sarah Ferko,
Jeffrey M. Abolafia		 source
presentation source		 15
PHUSE US 2025 Harnessing the Power of R Shiny in a GxP-Compliant and Validated Manner for Clinical Trial Use Sanyogeeta Andhale,
Shilpa Sood		 source
presentation source		 13
PHUSE US 2025 Optimising AI Software for Automated Protection of Personal and Commercially Sensitive Data Honz Slipka source
poster source		 7
PHUSE EU 2024 Guidance Beyond the SDTM Implementation Guide Kristin Kelly source
presentation source		 10
PHUSE EU 2024 Perl Regular Expressions in SDTM and ADaM Programming: Live Study Examples Pavol Valovic source
presentation source		 7
PHUSE EU 2024 Pre ADSL - Revolutionise Your ADaM Workflow Korak Datta,
Taniya Chatterjee		 source
presentation source		 8
PharmaSUG 2024 Advancing the Maturation of Standardized CRF Design Sugumaran Muthuraj,
Rubha Raghu		 source 9
PharmaSUG 2024 Bridging AI and Clinical Research: A New Era of Data Management with ChatGPT Illia Skliar source 12
PharmaSUG 2024 Guidance Beyond the SDTM Implementation Guide Kristin Kelly,
Michael Beers		 source 11
PHUSE US 2024 Beyond the Hype: A Pragmatic Approach to Leveraging AI/ML for Data Review Robert Musterer source
presentation source		 10
PHUSE US 2024 Codeless Queries: Harnessing AI to Translate Clinical Trial Questions into Custom Listings Through Intuitive UI Interactions Aditya Gadiko source
presentation source		 7
PHUSE US 2024 Guidance Beyond the SDTM Implementation Guide Michael Beers,
Blue Bell		 source
presentation source		 10
PHUSE EU 2023 How Can Python Be Used in Clinical Trials? Andrés Käsa,
Matt Davies,
Pierre Dostie		 source
presentation source		 21
PharmaSUG 2023 Have Meaningful Relationships: An Example of Implementing SDTM Special Purpose Data Set RELREC with a Many-to-Many Relationship Kaleigh Ragan,
Richann J. Watson		 source 11
PharmaSUG 2023 Patient's Journey using Real World Data and its Advanced Analytics Kevin Lee source 4
PHUSE US 2023 Beyond k-anonymity for Clinical Trial Data Anonymisation [presentation] Parvee Kumar,
Diwakar Angra		 source
video		 17
PHUSE EU 2022 Patient Narratives - Speeding Up Narrative Generation Using ODS Document Stores Neville Cope source
presentation source		 14
PHUSE US 2022 Using AI-based Technology to Accelerate Clinical Trial Data Sharing and Reuse [presentation] Ron Kaine,
Thomasin Element		 source
video		 33
PHUSE EU 2021 CDISC Analysis Results Standard Team: Enhancing Analysis Results and Traceability [presentation] Bess LeRoy,
Jeffrey M. Abolafia		 source
video		 41
PHUSE EU 2021 Engineering an MDR of the Future [presentation] Ali Dootson,
Mike Grove		 source
video		 19
PHUSE EU 2021 Navigating the Evolving Regulations for Health Canada [presentation] Gina Bennet source
video		 20
PHUSE EU 2021 Transforming Reporting - A Journey into Web Technology for Listing Generation [presentation] Joseph Rowley,
Kartik Rajan		 source
video		 23
PHUSE US 2021 CSR Narratives Automation [presentation] Ritesh Dhimmar source
video		 23
PHUSE US 2021 Using Natural Language Processing to Create Subject Safety Narratives [presentation] Frank Meloni,
Tim Willittes		 source
video		 8
PHUSE EU 2020 Advancing SDTM Annotation Through Automation [presentation] Anja Kreis,
Wolfgang Rohnert		 source
video		 20
PHUSE EU 2020 Novel eCRF Study Template to Support Adaptive Design Studies in Medidata Rave [presentation] Nele Claes,
Ray Lacchman		 source
video		 29
PHUSE EU 2020 The TransCelerate Hackathon: Accelerating Development [presentation] Johannes Ulander source
video		 26
PharmaSUG 2020 Natural History Study - A Gateway to Treat Rare Disease Tabassum Ambia source 5
PharmaSUG 2020 Untangling the Subject Elements Domain Christine McNichol source 8
PharmaSUG 2020 Updates in SDTM IG V3.3: What Belongs Where - Practical Examples Lucas Du,
William Paget,
Lingyun Chen,
Todd Case		 source 8
PharmaSUG 2020 Why Are There So Many ADaM Documents, and How Do I Know Which to Use? Sandra Minjoe source 10
PHUSE US 2020 Adverse Event and Treatment Emergent Approaches in the Industry Aimee Basile source
poster source		 11
PHUSE US 2020 Untangling the Subject Elements Domain Christine McNichol source
presentation source		 7
PHUSE EU 2019 Stuck in a Rut? Prakash Mistry source
poster source		 9
SGF 2019 Predicting Patients at High Risk of Hospital-Acquired Conditions Using the LOGISTIC Procedure Jennifer Hargrove,
Pamela Hipp,
Glenn Sidle		 source 12
PHUSE US 2019 DR3 - A Tool to Create Define-XML (SDTM/ADaM with ARM) [presentation] Eric Weising source 7
PHUSE EU 2018 CDISC Standards: Creating Clarity Out of Confusion [presentation] Kit Howard source 20
PHUSE EU 2018 Serious Adverse Events Identification: A Machine Learning Approach [presentation] Jingshu Liu,
Laura Katz		 source 37
PHUSE EU 2018 Stop Copying CDISC Standards Craig Parry source
poster source		 21
PHUSE EU 2018 Text as Data in the Context of Anonymising Clinical Study Reports Lukas Kniola,
Tim Perin		 source
presentation source		 12
PHUSE US 2018 Cue the Word - QC - All You Need to Know! Subha Jamburajan,
Nancy Haeusser		 source
presentation source		 6
PharmaSUG 2018 Core and Extension studies - Challenges and solutions towards SDTM submission Murali Marneni source 6
PharmaSUG 2018 Report Compatibility: System to evaluate your code against volatile sources. Joseph Cooney,
Randy Santiano,
Craig Brelage		 source 12
PharmaSUG 2018 Summary Table for Displaying Results of a Logistic Regression Analysis Lori S. Parsons source 9
SESUG 2017 Challenges and Solutions for Handling Re - screened Subjects in SDTM Charity Quick,
Paul Nguyen		 source 6
SESUG 2017 Statistician's secret weapon: 20 ways of detecting raw data issues Lixiang Larry Liu source 8
SESUG 2017 Using SAS to Proactively Monitor Drug Alerts: Implementing the URAC "Drug-Drug Interactions" Measure for a Specialty Pharmacy Karen E. Wallace source 8
PHUSE EU 2017 Clinical Study Oversight: Different Approaches to Using Data Standards Jasmine Kestermont,
Peter Van Reusel		 source
presentation source		 6
PHUSE EU 2017 Metadata-driven Tool for Creation of a Dataset for Exploratory Analyses Alexey Kuznetsov source
presentation source		 7
PHUSE EU 2017 SDTM Domains by Query - is it Possible? Johannes Ulander source
presentation source		 8
PHUSE EU 2017 Use of Fast Healthcare Interoperability Resources (FHIR) in the Generation of Real-World Evidence Trisha Simpson,
Regina Zopf		 source
presentation source		 12
PHUSE EU 2017 Visualizing and Cleaning Unsolicited Safety Data (ICSRs) Using R in Aiding Causality Assessment Sheik Akhil,
Krishna Asvalaya		 source
presentation source		 6
WUSS 2017 Using SAS to Proactively Monitor Drug Alerts: Implementing the URAC "Drug-Drug Interactions" Measure for a Specialty Pharmacy Karen E. Wallace source 8
PharmaSUG 2017 A Guide To Programming Patient Narratives Renuka Tammisetti,
Karthika Bhavadas		 source 6
PharmaSUG 2017 Statistician's secret weapon: 20 ways of detecting raw data issues Lixiang Larry Liu source 8
SESUG 2016 SDTM What? ADaM Who? A Programmer's Introduction to CDISC Venita DePuy source 9
PHUSE EU 2016 Assessing CDISC Therapeutic Area User Guides in a Machine Readable Format Johannes Ulander,
Niels Both		 source
presentation source		 4
PHUSE EU 2016 Use of Fast Healthcare Interoperability Resources (FHIR) in the Generation of Real World Evidence (RWE) Regina Zopf,
Jeffrey M. Abolafia,
Bhargava Reddy		 source
presentation source		 12
PharmaSUG 2016 AE: An Essential Part of Safety Summary Table Creation Rucha Landge source 12
PharmaSUG 2016 Associated Persons Domains - Who? What? Where? When? Why? How? Alyssa M. Wittle,
Michael Stackhouse		 source 6
PharmaSUG 2016 Automating Patient Narratives - The Medical Writer Loves Me! Scott Burroughs source 7
PharmaSUG 2016 Efficient Safety Assessment in Clinical Trials using the Computer-generated AE Narratives of JMP Clinical Richard C. Zink,
Drew Foglia		 source 13
PharmaSUG 2016 Prepare for Re-entry: Challenges and Solutions for Handling Re-screened Subjects in SDTM Charity Quick,
Paul Nguyen		 source 5
PharmaSUG 2016 The Power of Perl Regular Expressions: Processing Dataset-XML documents back to SAS Data Sets Joseph W. Hinson source 9
PHUSE EU 2015 Therapeutic Area Standards and their Impact on Current SDTM Implementations Johannes Ulander,
Niels Both		 source
presentation source		 6
PharmaSUG CN 2015 Hands-On ADaM ADAE Development Sandra Minjoe 7
PharmaSUG 2015 It Depends On Your Analysis Need Sandra Minjoe source 10
PharmaSUG 2015 Proc STREAM: The Perfect Tool For Creating Patient Narratives Joseph W. Hinson source 12
PharmaSUG 2015 Statistical Review and Validation of Patient Narratives Indrani Sarkar,
Bradford J. Danner		 source 5
SESUG 2014 SDTM What? ADaM Who? A Programmer's Introduction to CDISC Venita DePuy source 9
PHUSE EU 2014 ADaM Standards: What's New? Gavin Winpenny source
presentation source		 9
PHUSE EU 2014 Challenges with the Interpretation of CDIOSC - Who Can We Trust? Linda Palm Simonsson source
presentation source		 10
PHUSE EU 2014 Considerations in Creating Transparent SDTM-Based Datasets Jerry Salyers,
Richard Lewis		 source
presentation source		 8
PHUSE EU 2014 Data Transparency: Data De-identification and the Role of the Programmer [presentation] Jean-Marc Ferran source 20
PHUSE EU 2014 Standards Driven Innovation [presentation] Frederik Malfait source 36
MWSUG 2014 Jack of all Listings, A New Approach for Review of Clinical Data Hardik Panchal 15
PharmaSUG 2014 Hands-On ADaM ADAE Development Sandra Minjoe,
Kimberly Minkalis		 source 7
NESUG 2013 The ADaM Solutions to Non-endpoints Analyses Chengxin Li 12
PharmaSUG 2013 Hands-On ADaM ADAE Development Sandra Minjoe source 7
PharmaSUG 2013 Pretty Please?! Making RTF Output "Pretty" with SAS Carol Matthews,
Elena Kalchenko		 source 10
PharmaSUG 2013 Taking a Census in Utero: An Introduction to Pregnancy Registries with an Emphasis on Identifying Multiple Gestations Britney D. Gilbert source 8
SGF 2013 Using the ADaM ADAE Structure for Non-AE Data Mario Widel,
Sandra Minjoe		 source 13
PHUSE EU 2012 Interpreting ADaM Standards with OpenCDISC Trupti Bal,
Madhura Paranjape		 source
presentation source		 8
SESUG 2012 Developing a Complete Picture of Patient Safety in Clinical Trials Richard C. Zink,
Russell D. Wolfinger		 source 5
SESUG 2012 Diverse Report Generation With PROC REPORT Diverse Report Generation source 6
MWSUG 2012 Programmed Assisted Patient Narratives (PANs) with New SAS ODS and Graphical Approaches Faye Yeh,
Melvin S. Munsaka		 12
WUSS 2012 Modular processing for Prep-to-research anaylsis - interfacing XML SAS and Microsoft Excel David Tabano source 16
PharmaSUG 2012 Accessing Microsoft Excel Workbook Cell Attributes from within SAS v9 Timothy J. Harrington source 9
PharmaSUG 2012 Diverse Report Generation With PROC REPORT Chris Speck source 6
PharmaSUG 2012 Supplementing Programmed Assisted Patient Narratives (PANs) with Graphs Using SAS Faye Yeh,
Melvin S. Munsaka		 source 12
PHUSE EU 2011 Three Unique Case Studies - On the Trail of the Holy Grail of SDTM Implementation Kenneth Stoltzfus source
presentation source		 6
NESUG 2011 Generating Define.xml Sandeep Kottam,
Uma Sarath Annapareddy,
Sree Lakshmi Kalyani Tripuraneni		 20
NESUG 2011 Product Repository: Oblectives and Utilization - A Case Study Amit Bhanose,
Smitha Mullapudi		 5
PharmaSUG 2011 Analytical Methods for Post-Marketing Safety Surveillance Annette Stemhagen,
Juliane K. Mills		 source 3
PharmaSUG 2011 From SAP to BDS: The Nuts and Bolts Nancy Brucken,
Paul K. Slagle		 source 9
PharmaSUG 2011 The Illusion of Good Data, or How Not to Think of a Blue Elephant Kim Truett source 6
NESUG 2010 Producing Listings and Reports Using SAS and Crystal Reports Krishna (Balakrishna) Dandamudi 18
PharmaSUG 2010 CDASH Standards for Medical Device Trials: CRF Analysis Parag Shiralkar,
Jennie Tedrow,
Kit Howard,
Laura Fazio,
Daniela Luzi,
Rhonda Facile		 8
MWSUG 2009 Dietary Glycemic Load and Risk of Colon Cancer: A Guide to Data Management Svetlana Zelenskiy,
Lauren Byrne,
Cheryl L. Thompson,
Thomas C. Tucker,
David Bruckman,
Li Li		 16
NESUG 2009 A Practical Introduction to implementing the Clinical Data Acquisition Standards Harmonization (CDASH) standards Jennifer Price 7
NESUG 2009 Tips of Using Proc Report For Summary Tables And Listings Jenny H. Zhang 6
PharmaSUG 2009 A Practical Introduction to Clinical Data Acquisition Standards Harmonization (CDASH) Jennifer Price 5
PharmaSUG 2009 Converting the define.xml to a Relational Database to Enable Printing and Validation [presentation] Lex Jansen 76
PHUSE EU 2008 A Graphical Approach to Examine the Completeness of Epidemiological Data: Patient Profile Plots (PPPs) and Centre Profile Plots (CPPs) Methodios Typou,
Joseph Kim		 source 14
PHUSE EU 2008 Automated Drug Safety Signal Detection with Guided Ana Eric C. Brinsfield,
David Olaleye		 source 7
PharmaSUG 2008 %CHCKFRQS - A Macro Application for Generating Frequencies for QC and Simple Reports John Iwaniszek,
Natalie Walker,
Laura Lovette		 8
PharmaSUG 2008 Experiences Submitting CDISC SDTM and Janus Compliant Datasets Carol Vaughn,
Gregory Ridge,
William Friggle		 10
NESUG 2007 Producing Listings and Reports Using SAS and Crystal Reports Krishna (Balakrishna) Dandamudi 18
PharmaSUG 2007 Automatic Creation of Analysis Datasets for Clinical Trials - A Macro Program John H. Adams 17
PharmaSUG 2007 Combining ODS Output Datasets to Increase Program Clarity and Reduce Macro Load Rod Norman 7
PHUSE EU 2006 Statistical Graphics and Reporting in Drug Development Michael O'Connell,
Sven Knudsen		 source 13
SESUG 2006 A Relational Understanding of SDTM Tables John R. Gerlach source 10
NESUG 2006 Using PROC CDISC Chauthi Nguyen 5
PHUSE EU 2005 Understanding the Japanese culture and approval process Richard Harvey source 10
PharmaSUG 2005 %PREFTAB - A macro to automatically create adverse event, medical history and concomitant medication tables Wilfried Esken 11
PharmaSUG 2005 Programming and Data Differences Between Clinical Trials and Observational Studies Margaret M. Coughlin 6
PharmaSUG 2004 Use That SAP to Write Your Code Sandra Minjoe 9
NESUG 2003 Date/Time Stamped Files and Audit Trails: What Part 11 Compliant SAS Systems are Made Of Carolyn Dougherty 11
SEUGI 2003 Drug Approval, making the best treatments available safely, but quickly - using SAS at the heart of generic reporting systems. [presentation] Jonathan Chainey,
Rob Horton		 source 25
SEUGI 2000 Creating PDF Documents including hyper-links, bookmarks and a table of contents with the SAS Software [presentation] Lex Jansen source 39
SUGI 1998 Individual Summaries: Bigger Needles in Smaller Haystacks Joel J. Gruenke source 5
SEUGI 1997 Data Mining and SAS/SPECTRAVIEW software: a case study Annie Postic,
Bengt Bengtsson		 source 36
MWSUG 1996 A Macro to Estimate Morbidity Indices Laurel A. Panser,
Janice R. Offord,
James M. Naessens,
Mary E. Campion,
Sherine E. Gabriel		 8
SUGI 1993 Using the SAS System in the Pharmaceutical Industry: Project Setup and Standardization for the Analysis of Clinical Trial Data. Cam Huffman,
Carl Arneson,
John Horton,
John Henry King		 source 5
SUGI 1990 Using SAS/AF Program Screens to Create a Program Manager/ Document Producer for Data Editing Robin L. Wright,
Charles W. Kish Jr.,
Wayne M. Cannon,
Chris Bullard,
David Martinez		 source 6
SUGI 1984 THECIS-The Clinical Information System Judith A. Burns,
Leon T. Hairie,
Thomas R. Hoffman		 source 6

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