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clinical database

108 papers and 13 presentations; 117 titles.

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Conference × Year × Title × Authors Extras Pages
PharmaSUG 2026 Traceability in Real World trials - just an aERD away. Ashwini Yermal Shanbhogue source 7
PHUSE EU 2025 How to map lab data into the LB domain and ADLB Bert Parmet source
poster source		 6
PharmaSUG 2025 Data management and biostatistics synergy: how to achieve and what can be expected Diana Avetisian source 11
PHUSE US 2025 Automating your safety data reconciliation: An approach towards reliable and efficient SAE reconciliation process Ritu Dogra source
presentation source		 11
PHUSE US 2025 Data Transformation: Achieving Compliance with Irregular Data Reyes Eduardo Elizalde Duarte source
presentation source		 6
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 eProtocol and the Promise of Automation Bill Qubeck,
Suhas Giriraj		 source
presentation source		 17
PHUSE US 2025 Innovative Data Cleaning to Prevent Unblinding Errors in Double-Blind Trials Ling Zhang,
Nan Zhou		 source
presentation source		 4
PHUSE US 2025 Wearable Technology: Enhancing Patient Monitoring and Real-World Evidence Bill Qubeck,
Sridhar Vijendra		 source
presentation source		 15
PHUSE EU 2024 Enhancing Quality of External Data Pascale Youinou source
presentation source		 6
PharmaSUG 2024 Game changer! The new CDISC ADaM domain ADNCA for PK/PD data analysis Santosh Ranjan source 7
PHUSE US 2024 Digital Protocol Vision ... How Digital Information Can Transform and Automate Our Processes [presentation] Bill Qubeck,
Chris Decker		 source 27
PHUSE EU 2023 Data Managers and R Programming: The Unlikely Pair Anaelle Perretti (Bonetta) source
presentation source		 9
PHUSE US 2023 Reviewing External Vendor Data Transfer Specifications from a Programming Standpoint Mahesh Minnakanti source
presentation source		 5
PHUSE EU 2022 Clinical Data Standards and Production of SDTMs. Are We Missing Important Points? [presentation] Eva Stigson,
Paulina Kuczkowska		 source 15
PHUSE EU 2021 iListing - Get More Out of Listings [presentation] Katja Glass source
video		 37
PHUSE EU 2021 Standing Room Only: RW08: The Convenient Structure of the OMOP CDM [presentation] George Allerston,
Khaleeq Mannan		 source 20
PHUSE US 2021 AI Powered Decision Support Systems with Wearable Sensors for Remote Patient Monitoring in Clinical Trials [poster] Surabhi Dutta source 1
PHUSE US 2021 Standing Room Only Presentation: DH02: On the Other Side of the Fence: When Two Skill Areas Join Forces and Boundaries Dissolve [presentation] Mette Krogh Beyer,
Stine Ross		 source 15
PharmaSUG 2021 BIMO SAS Macros and Programming Tools Mi Young Kwon,
Rohit Kamath		 source 12
PharmaSUG 2020 Clinical Database Metadata Quality Control: Two Approaches using SAS and Python Craig Chin,
Lawrence Madziwa		 source 16
PharmaSUG 2020 Preparing a Successful BIMO Data Package Elizabeth Li,
Carl Chesbrough,
Inka Leprince		 source 20
PHUSE US 2020 A Programmer's Journey through the BIMO Submission Process Raghavender Ranga source
presentation source		 12
PHUSE US 2020 Adverse Event and Treatment Emergent Approaches in the Industry Aimee Basile source
poster source		 11
PHUSE US 2020 Natural Language Processing for Enhanced Treatment Decision Phani Ponnapalli,
Subrahmanyam Rayaprolu		 source
presentation source		 10
PHUSE EU 2019 Semi Auto-generated Narratives Bjarke Klein source
presentation source		 7
PHUSE EU 2019 Using R Shiny to Create an Interactive Visualisation Patient Profile Elva Chen,
Brian Munneke		 source
presentation source		 8
PharmaSUG 2019 The Anatomy of Clinical Trials Data: A Beginner's Guide Venky Chakravarthy source 14
PHUSE EU 2018 Handling CRF Design Changes in a Live Environment Andre Snelting,
Nieke De Ruiter		 source
presentation source		 10
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 Identification of New Information in a Data Based on a Data Point Level Eric Kammer,
Thomas Binnen		 source
presentation source		 3
PHUSE US 2018 SDTM: It is Not all Black and White Swapna Pothula,
Roman Radelicki		 source 7
PHUSE US 2018 Secure Data Office: An Independent Team that Can Come to the Rescue in Blinded Trials Annelies Van Zeveren,
Yana Hoorne		 source
presentation source		 9
PharmaSUG 2018 Automate Clinical Trial Data Issue Checking and Tracking Krishna Avula,
Dale LeSueur		 source 5
PharmaSUG 2018 Preventing premature unblinding in PK/PD related studies Debbie Sisco,
Alice Zong		 source 11
PharmaSUG 2018 Second Primary Malignancy (SPM) Analyses in a Disease Registry Study Jane Lu,
Shankar Srinivasan,
Robert Knight		 source 6
SGF 2018 Automation of Clinical Trial Result Posting to ClinicalTrials.gov and EudraCT Sherry Meeh source 9
SGF 2018 The Anatomy of Clinical Trials Data: A Beginner's Guide Venky Chakravarthy source 14
PHUSE EU 2017 KeyDAN: a Clinical Data De-identification Solution Stéphane Chollet source
presentation source		 4
PHUSE EU 2017 The Secure Data Office Concept Annemie Van Dijck source
presentation source		 9
PharmaSUG 2017 Clinical and Vendor Database Harmony; Can-t we all just get along? Brian Armstrong,
Renee Kerwin		 source 9
PHUSE EU 2016 Integrating the New EMA Requirements on Public Disclosure in the Study Conduct [presentation] Jean-Marc Ferran source 20
SGF 2016 An Efficient Algorithm in SAS to Reconcile Two Different Serious Adverse Event (SAE) Data Sources Zhou Hui source 7
PHUSE EU 2015 CodEX - When Excel Meets SAS to Code Clinical Data Stéphane Chollet,
Cathy Scoupe		 source
presentation source		 8
PharmaSUG 2015 The Disposition Table: Make it Easy Endri Endri,
Benedikt Trenggono		 source 10
PharmaSUG 2015 Use of SAS Reports for External Vendor Data Reconciliation Soujanya Konda source 12
PHUSE EU 2014 From ODM to SDTM: An End-to-End Approach Applied to Phase I Clinical Trials Alexandre Mathis source
presentation source		 5
PHUSE EU 2014 Implementation of Oncology Specific SDTM Domains Jacintha Eben source
presentation source		 8
PharmaSUG 2014 Linking Healthcare Claims and Electronic Health Records (EHR) for Patient Management - Diabetes Case Study Paul A. LaBrec source 17
SGF 2014 Converting Clinical Database to SDTM: The SAS Implementation Hong Chen source 5
PHUSE EU 2013 EDC Integration [presentation] Rob Jongen source 21
PHUSE EU 2013 Supporting End to End Standards in Study Setup Anna Louise Wilson source
presentation source		 5
PHUSE EU 2013 The Great Outdoors - (Using SAS External File and SAS File 1/0 Functions) [presentation] Lawrence Heaton-Wright source 25
NESUG 2013 Merging SAS Programming Groups: Phased-in Approach Margaret M. Coughlin,
Alfredo Rojas		 5
PharmaSUG 2013 A Simple Approach to the Automated Unit Testing of Clinical SAS Macros Matthew Nizol source 12
PharmaSUG 2013 Be a Dead Cert for a SAS Cert: How to prepare for the most important SAS Certifications in the Pharmaceutical Industry Hannes Engberg Raeder source 10
PharmaSUG 2013 Managing 21 CFR Part 11 Compliance: Using Checksums on Opens Systems Carey G. Smoak,
Mario Widel		 source 8
PharmaSUG 2013 SDTM Harmonization in the Absence of CDASH - A Modularized Approach to Domain Programming Annie S. Guo source 12
SGF 2013 Running SAS Programs Using Skype Romain Miralles source 6
PHUSE EU 2012 Spotting DILI for FDA Submission Nicola Tambascia,
Sven Greiner		 source
presentation source		 7
PharmaSUG 2012 Using Skype to run SAS programs Romain Miralles source 6
PHUSE EU 2011 FDA CDER Common Data Standards Issues: Evolution of SDTM Submission Standards Peter Van Reusel,
Tina Apers		 source
presentation source		 3
PharmaSUG 2011 An Excel Framework to Convert Clinical Data to CDISC SDTM Leveraging SAS Technology Sophie McCallum,
Stephen Chan		 source 12
WUSS 2010 An Excel Framework to Convert Clinical Data to CDISC SDTM Leveraging SAS Technology Ale Gicqueau source 12
PHUSE EU 2010 Clinetics Data Merge - A Platform for Exchange of Pharmacokinetic Data Ralf Schefer-Pregi,
Andreas Schwarzer		 source
presentation source		 5
PHUSE EU 2010 Electronic transfer of sAE to Global Pharmacovigilance Eva Bervar source
presentation source		 5
PHUSE EU 2010 Modeling and Simulation: challenges for the clinical programmer and for the group leader [presentation] Vincent Buchheit source 18
PHUSE EU 2010 Traceability between SDTM and ADaM converted analysis datasets Florence Somers,
Michael Knoessl		 source
presentation source		 7
PharmaSUG 2010 Evolving role of statistical SAS programmers in the pharmaceutical industry Venkata Sekhar Bhamidipati,
Haiping Zhou		 5
PharmaSUG 2010 Smart Programming and SAE Reconciliation Haibin Shu,
Ronen Mansuri,
Maggie Ci Jiang		 3
PharmaSUG 2010 Utilizing SAS to Dynamically Generate Clinical Trial Data Transformation Programs Clark Peirce,
Johnny Johnson		 7
PHUSE EU 2009 Building and maintaining a clinical data warehouse - challenges and opportunities for pharmaceutical programmers [presentation] Juergen Kuebler source 15
PHUSE EU 2009 Clinical Database acceptance: what statistical review checks are necessary to validate a database? Genevieve Jehl source 12
PharmaSUG 2009 Oracle Clinical for SAS Programmers Kevin Lee 8
WUSS 2008 Using SAS/AF for Managing Clinical Data Wynn Zheng source 14
PHUSE EU 2008 Improving the Quality of Data Ester Schoeman source 7
SGF 2008 Oracle Clinical for SAS Programmers Kevin Lee source 8
NESUG 2007 Oracle Clinical for the SAS Programmer Kevin Lee 9
PHUSE EU 2007 Clinical Research Information Management... David Handelsman source 8
PHUSE EU 2007 Having your cake & eating it: extracting data and attrib from OC John Hendrickx source 17
PHUSE EU 2007 LSLV to Final CSR Tables in 24 hours - Dream or Reality? Stinder Fowler source 10
PHUSE EU 2007 PK data file(s) creation process Ann Cuijpers,
Hilde Wuyts		 source 3
PharmaSUG 2007 A Scalable Platform For Clinical Trials - Interoperability And Automation In A Web-Based Environment John R. Gerlach,
Maulik Shah		 11
PharmaSUG 2007 Managing the CRO Relationship to Effectively Request and Receive CDISC STDM and ADaM Deliverables Kenneth Eng,
David C. Izard,
Terek J. Peterson		 8
SESUG 2006 Data Mining of Dental Information Christiana Petrou source 7
WUSS 2006 An Approach Finding the Right Tolerance Level for Clinical Data Acceptance Karen Walker source 5
PharmaSUG 2006 De-Identification of Clinical Trials Data Demystified Jack Shostak 12
PHUSE EU 2005 CLIREV - A friendly and flexible Clinical Data Review Tool Angelo Tinazzi source 6
PHUSE EU 2005 Customer oriented CDISC implementation Edelbert Arnold,
Ulrike Plank		 source
poster source		 13
PharmaSUG 2005 An Approach Finding the Right Tolerance Level for Clinical Data Acceptance Karen Walker 6
NESUG 2004 Clinical Trial Data Validation: Using PROC SQL Effectively Balakrishna Dandamudi 20
NESUG 2004 Extracting Data from Oracle into SAS - Lessons Learned Maria Y. Reiss 12
PNWSUG 2004 Extracting Data from Oracle into SAS - Lessons Learned Maria Y. Reiss 12
PharmaSUG 2004 A SAS Macro for Rapid Identification of Missing Data Records Kim Truett 7
PharmaSUG 2004 Automating the Documentation of Oracle Clinical Database Specifications Kyle McBride 9
PharmaSUG 2003 Use of Text Miner to Automatically Abstract Patient Information from the Pharmacy Order Database Patricia B. Cerrito,
Antonio Badia,
John C. Cerrito,
James A. Cox		 6
SUGI 2003 Why SAS is the Best Place to Put Your Clinical Data Steven A. Wilson source 6
PharmaSUG 2002 Serology Inventory System Mariya Charny 8
NESUG 2001 Using SAS/Warehouse Administrator., Enterprise Guide., and Enterprise Reporter. to Manage and Access a Clinical Data Warehouse Theresa J. Kelso 3
SUGI 2001 Data Modeling in Clinical Data Analysis Projects Gajanan Bhat source 6
NESUG 2000 Clinical Trial Laboratory Data Management using the SAS System Marianne Hack 5
PharmaSUG 2000 Data Modeling in Clinical Data Analysis Projects Gajanan Bhat 3
NESUG 1999 Are We Done Yet? Tracking Your Data Management Process with SAS Software Daphne E. Ewing,
Barbara McLaughlin		 4
SEUGI 1999 Clinical processes and SAS/PH-Clinical, a good marriage? [presentation] Patrick Genyn source 24
SEUGI 1999 Developing a SAS data management system using FRAME technology [presentation] David Smith,
Sandy Meek		 source 33
SEUGI 1998 Knowledge Discovery and Data Mining on the Example of Clinical Databases Leon Bobrowski,
Magdalena Topczewska		 source 6
WUSS 1997 Using SAS as a Clinical Data Repository Carl R. Haske source 6
SEUGI 1997 Point-and-click data validation using SAS/AF software Leif Puddefoot source 9
PharmaSUG 1997 A SAS/AF Class Library for Automated Generation of Clinical Report Programs Carl R. Haske 7
PharmaSUG 1997 Clinical Software Systems Development in SAS/AF Carl R. Haske 11
SUGI 1997 Using SAS/AF for Managing Clinical Data Carl R. Haske source 6
SESUG 1996 Developing Clinical Software Systems in SAS/AF Carl R. Haske 10
MWSUG 1996 Clinical Data Management Using SAS/AF Carl R. Haske 8
SUGI 1996 An Integrated Clinical Data Management System in SAS Carl R. Haske source 6
SUGI 1996 Choosing an Application Development Tool for Your CANDA Barry R. Cohen source 8
NESUG 1995 The Choice of SAS Software as the Application Development Tool for Your CANDA Barry R. Cohen 9
SUGI 1995 Database Specifications and Data Dictionary System Ala Majid Sweidan,
Bernd Doetzkies		 source 4
SEUGI 1991 Developing Reporting Systems for Clinical Trials in the Pharmaceutical Industry David J. Shannon,
Mark Baillet		 source 12
SEUGI 1990 SAS Software Version 6.06, Beta-test under VMS - 4 Months User Experience Stephen J. Burman source 6
SEUGI 1989 Design And Implementation Of Clinical Data Management Applications On A PC Network Mark Crawford source 12
SUGI 1988 Integration of ORACLE and the SAS System in the Generation of Adverse Experience Reports Chih-Wu Chang,
Edward F.C. Pun		 source 5

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