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372 papers and 72 presentations; 419 titles.

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Conference × Year × Title × Authors Extras Pages
PharmaSUG 2026 An Agentic AI Framework That Reads Statistical Analysis Plans and Generates TFL Table of Contents Siqi Wang,
Toshio Kimura,
Songgu Xie,
Weiming Du		 source 6
PharmaSUG 2026 Early Restricted Unblinded PK Data Access (ERUPA): Framework to Accelerate PopPK and ERES Deliverables Through Data-Centric, Firewalled Workflows Dheeraj Rupani,
Srinivas Bachina,
Kiran Kumar Kode		 source 7
PharmaSUG 2026 From Programmer to Influencer: Strategic Leadership for Statistical Programmers in Clinical Development Xiaohan Zou,
Wei Shao,
Yi Yan		 source 9
PHUSE US 2026 AI Reading and Understanding the SAP to Generate the TFL TOC Siqi Wang,
Toshio Kimura		 source
presentation source		 6
PHUSE US 2026 AI Won't Replace Leaders-But It Will Redefine Them [presentation] Chris Decker source 9
PHUSE US 2026 End-to-End Workflow for CDISC Estimand Framework in Clinical Trials Hiral Raval,
Simon Luo		 source
poster source		 12
PHUSE US 2026 Submitting RWD: Where We Are and Where We Are Going Ingeborg Holt,
Sarah Ferko,
Jeffrey M. Abolafia		 source
presentation source		 24
PHUSE US 2026 The Journey Beyond Anonymisation: Exploring the Secondary Use of Clinical Trial Data Yuliia Cherednichenko,
Tetiana Skorokhod		 source
presentation source		 18
PHUSE US 2026 The Revolution of Digitised Study Designs: Standards, Use Cases and Tools Berber Snoeijer source
presentation source		 3
PHUSE APAC 2026 Bridging the Divide: Harmonizing HL7 FHIR, OMOP, and CDISC Standards for Regulatory-Grade Real-World Evidence Yasa Sreekanth Reddy source
presentation source		 9
PHUSE APAC 2026 Embracing the Semantic Shift: SDTMIG 4.0 and the Rise of Intelligent Clinical Data Standards Binitha Sathyabhama,
Venkateswarlu Layam		 source
presentation source		 6
PHUSE EU 2025 Close Encounters with Real-World Data Jeffrey M. Abolafia,
Sarah Ferko,
Ingeborg Holt		 source
presentation source		 21
PHUSE EU 2025 Decode Your Future: A Professional Development Growth Map for Programmers and Statisticians by Role Type Diana Stuart source
poster source		 8
PHUSE EU 2025 From Standards to Strategy: Customising CDISC Open Rules for the TMF Reference Model [presentation] Irina Sargsyan,
Sabine Jonas		 source 20
PHUSE EU 2025 The Kids Are All Right: How Investing in Career-Young Talent Can Create Engaged Future Leaders Sean Miles source
presentation source		 3
PHUSE EU 2025 The Value of Clinical Trial Data: From Submission to Innovation Anne Katrine Alsing source
presentation source		 8
PharmaSUG 2025 Change the way you think of Codelist - Optimize managing Organization Controlled Terminology with a meta-model and its features to manage Codelist in MDR Kairav Tarmaster source 11
PharmaSUG 2025 Decoding the Role of Statistical Programming - A Decade of Keytruda Submissions and Approvals Mary N. Varughese,
Hong Qi		 source 8
PharmaSUG 2025 Enhancing Dictionary Management and Automation with NCI EVS: A Deeper Dive for the CDISC Community Anthony Chow source 6
PharmaSUG 2025 Scoring Real-World Data Reliability for Clinical Investigations James Joseph source 15
PharmaSUG 2025 SDTM Transformation through Artificial Intelligence (AI) and Human in the Loop (HITL): Lessons Learnt from Abbvie Case Study Aman Thukral,
Sanjay Bhardwaj		 source 2
PharmaSUG 2025 The Model Maketh the Metadata Carlo Radovsky source 19
PHUSE US 2025 Collaborating on Standards: An Approach to Harmonizing Vaccine Regulatory Submissions Fred Bermont,
Médéric Celle,
Estella Sani,
Erin Gnas,
Jennifer Mastri,
Leslie Morgan,
Naila Musani,
Ramana Setty,
Sandra VanPelt Nguyen,
Yun Zhang		 source
presentation source		 8
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 End-to-End Therapeutic Area Data Standards Development and Governance - A Case Study Involving CRS and ICANS Yaling Teng source
presentation source		 7
PHUSE US 2025 Future-Proofing Clinical Data Standards: Preparing for AI and Machine Learning Shivoy Pandita source
presentation source		 8
PHUSE US 2025 Mapping OMAP Data to SDTM - Use Case for RWD in CAR-T Registry Studies Kai Deng,
Joe Xi		 source
presentation source		 5
PHUSE US 2025 Solving real-world data (RWD) reliability challenges for use in regulatory decision-making Tasha Nagamine source
presentation source		 5
PHUSE EU 2024 Connecting Standard from Design to Analysis to Submission: Finishing the CDISC 360 Vision [presentation] Peter Van Reusel source 25
PHUSE EU 2024 Considerations for the Submission of RWD using CDISC with Insights from HL7 FHIR and OMOP Jeffrey M. Abolafia,
Sarah Ferko,
Ingeborg Holt		 source
presentation source		 13
PHUSE EU 2024 Database Lock Is Only the Beginning: The Long, Winding Journey of Secondary Data Reuse at Roche Tamara Senior source
presentation source		 3
PHUSE EU 2024 Digital Data Flow: Achieving Protocol Digitalisation and Clinical Research Interoperability Through Multi-Stakeholder Collaboration [presentation] Mikkel Traun,
Lakshmi Sankar		 source 21
PHUSE EU 2024 From Source to Submission: Getting the Best of Multiple Standards Jules Van der Zalm,
Berber Snoeijer		 source
presentation source		 4
PHUSE EU 2024 Harmonising FDA and PMDA Submission Requirements Luca Semeraro source
presentation source		 12
PHUSE EU 2024 ID-SPECTACKLE: Making ADaM specifications "Fun" Sophie Dekeyser source
presentation source		 11
PHUSE EU 2024 OAK Productivity Experiment - How We Made SDTM Programming 5x Faster Amy Franklin,
Magdalena Krochmal		 source
presentation source		 5
PHUSE EU 2024 Standards Implementation with a Knowledge-Driven, AI-Powered Platform Roger Gagali Angoh source
presentation source		 3
PHUSE EU 2024 Synthesised Real-world Data: JSON and the Argonauts Anil Sekhari source
presentation source		 10
PHUSE EU 2024 The Significance of Generic Data Transfer Specification for Non-CRF Data in Clinical Trials Samaneh Sabiani,
Kristina Zweier		 source
presentation source		 9
PHUSE EU 2024 Transcriptomics - A Demanding Data Analysis that Expands the Limits of Regulated Clinical Data Handling Lea Yoshida Hildebrandt source
presentation source		 6
PharmaSUG 2024 Automating third party data transfer through digitized Electronic DTA Management Vandita Tripathi,
Manas Saha		 source 6
PharmaSUG 2024 Interfacing with Large-scale Clinical Trials Data: The Database for Aggregate Analysis of ClinicalTrials.gov Joshua J. Cook,
Achraf Cohen		 source 16
PharmaSUG 2024 Reimagining reporting and Visualization during clinical data management Vandita Tripathi,
Manas Saha		 source 9
PharmaSUG 2024 Study Start Date - Let-s Get it Right! David C. Izard source 6
PHUSE US 2024 Demystifying Submissions to NMPA China [presentation] Hiral Raval,
Dyuthi Yellamraju		 source 19
PHUSE US 2024 Future Clinical Data Submission Standards: CDISC, FHIR, OMOP, or Hybrid Model Jeffrey M. Abolafia,
Sarah Ferko,
Ingeborg Holt		 source
presentation source		 10
PHUSE US 2024 Incorporating Real-World Data in a Low-Interventional Study: Challenges and Considerations Sandra VanPelt Nguyen source
presentation source		 8
PHUSE US 2024 Scaling ECAs from Projects to the Enterprise: Multicentre, Multisource Infrastructure for External Control Arms Jussi Leinonen,
Mayur Saxena		 source
presentation source		 4
PHUSE US 2024 The TransCelerate/CDISC Digital Data Flow Project: Practical Electronic Study Designs [presentation] David Iberson-Hurst source 28
PHUSE US 2024 Unlocking the Future of Tables with the {tfrmt} R Package Becca Krouse source
presentation source		 8
PHUSE US 2024 Usage of OMOP-CDM along with CDISC in Clinical Trials: Challenges and Opportunities Parag Shiralkar source
presentation source		 5
PHUSE EU 2023 Generalisable Analysis Pipelines for Handling Large HTA Submissions [poster] Nicolai Skov Johnsen,
Matthew Phelps		 source 1
PHUSE EU 2023 Practical Operations of Electronic Study Data Submissions Priyanka Pujari source
presentation source		 9
PHUSE EU 2023 The TransCelerate/CDISC Digital Data Flow Project: Practical Electronic Study Designs [presentation] David Iberson-Hurst source 28
PharmaSUG 2023 Automation of the SDSP CBER Appendix for Vaccine Studies Nicole Jones,
Pritesh Solanki		 source 6
PharmaSUG 2023 CDISC Conformance and Compliance: So Many Resources, So Little Time! Jennifer K. Fulton,
Stephen Black		 source 11
PharmaSUG 2023 Challenges with Metadata Repository System Implementation: A Sponsor-s Perspective Radhika Kale,
Reema Baweja		 source 9
PharmaSUG 2023 Digital Data Flow (DDF) and Technological Solution Providers Prasoon Sangwan,
Piyush K. Singh		 source 8
PharmaSUG 2023 FDA's Study Data Policy Framework and How CDISC Properties Are Evaluated for Inclusion Helena Sviglin source 20
PharmaSUG 2023 OCS Update: OCS Clinical Services & the Traceability Assessment Jesse Anderson source 25
PharmaSUG 2023 U.S. Conference Liping Sun source 22
PHUSE US 2023 Best Practice for Successful Adoption and Implementation of CDISC Data Standards [presentation] Gilbert Hunter,
Martin Johnston		 source
video		 25
PHUSE US 2023 Computerised Algorithm for Multiple Myeloma Response Assessments Mahesh Swaminathan source
presentation source		 3
PHUSE US 2023 Data Standards Governance and Implementation Across Industry: Key Challenges and Benefits [presentation] Gayathri Mahadevan,
Matt Baldwin		 source
video		 15
PHUSE US 2023 Enabling the Digital Data Flow from eProtocol to Downstream Processes [presentation] Berber Snoeijer,
Kumar Patel		 source
video		 13
PHUSE EU 2022 Breaking Down the Data Standards Silos - A New Metadata Ontology for Data Analysis Derivations Chris Price,
Nelia Lasierra		 source
presentation source		 7
PHUSE EU 2022 Clinical Data Standards and Production of SDTMs. Are We Missing Important Points? [presentation] Eva Stigson,
Paulina Kuczkowska		 source 15
PHUSE EU 2022 Devices and Decentralised Clinical Trials Using a Storage and Advanced Analytics Platform for the Clinical Data Environment (ALYCE) [presentation] Stephan Cichos,
Anja Thiede		 source
video		 23
PHUSE EU 2022 Governance and Cataloguing of Analytics Assets [presentation] Paul McCaffery,
Clement Benemara		 source 15
PHUSE EU 2022 The Secret to Getting Your Dream Job Offer [presentation] Tom Oades source
video		 13
PHUSE EU 2022 Using Individual-level Real-world Data to Inform Disease Area Data Models Employed for Clinical Trial Simulation and Design [presentation] Sheila McCartan source
video		 41
PharmaSUG 2022 RWD (OMOP) to SDTM (CDISC): A primer for your ETL journey Ashwini Yermal Shanbhogue source 10
PHUSE EU 2021 AI-powered Drug Development: Accelerating Trials with AI & ML [presentation] Raj Indupuri source
video		 10
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 EMA Panel Discussion: What Might the Future Landscape of Submitting Data Look Like in 2025 ? [presentation] Eftychia-Eirini Psarelli,
Jesper Kjær		 source 14
PHUSE EU 2021 EMA Panel Discussion: What Might the Future Landscape of Submitting Data Look Like in 2025 ? [presentation] Eftychia-Eirini Psarelli,
Jesper Kjær		 source 11
PHUSE EU 2021 Next Generation MDR Solution for Study Design and Configuration Using Concept-based Standards [presentation] Mikkel Traun source
video		 15
PHUSE US 2021 An R-based Tool to Build Questionnaires, Ratings and Scales (QRS) in EDC for Clinical Trials [presentation] Catherine Abogado,
Rammprasad Ganapathy		 source
video		 19
PHUSE US 2021 COVID-19 Outbreak Visualization Using a Clinical Data Science Platform [presentation] Iryna Kotenko,
Sergey Glushakov		 source
video		 15
PHUSE US 2021 How to Submit Study Data to Comply with Technical Rejection Criteria [poster] Lina Cong source 1
PHUSE US 2021 How Will Knowledge Graphs Improve Clinical Reporting Workflows? [presentation] Alexey Kuznetsov,
Jorine Putter		 source 9
PHUSE US 2021 Open-Source Development for Traditional Clinical Reporting [presentation] Michael Stackhouse,
Nathan Kosiba		 source
video		 12
PHUSE US 2021 Real-Time Clinical Trial Analytics Using Automation with IBM Clinical, Medidata Rave and Datacise [presentation] Amritpal Singh source
video		 10
PHUSE US 2021 Regulatory Update & Townhall [presentation] Ethan Chen source 28
PharmaSUG 2021 FDA Study Data Technical Rejection Update [presentation] Ethan Chen source 36
PharmaSUG 2021 SEND for CBER Lisa Lin source 26
PHUSE EU 2020 Digital Data Flow - A Solution for Study Start-up and Amendments [presentation] Palanipandiyan Chokkalingam,
Srinivasan Mahalingam		 source
video		 22
PHUSE EU 2020 Graph Data Representation - The FAIRest of Them All [presentation] Eva Kelty,
Peter Tormay		 source
video		 25
PHUSE EU 2020 Implementing FAIR in OHDSI: Challenges and Opportunities in EHDEN [presentation] Tess Korthout source
video		 23
PHUSE EU 2020 SUPPQUAL Datasets: The Good, the Bad and the Ugly [presentation] Sergiy Sirichenko source
video		 40
PHUSE EU 2020 Understanding the Spread of COVID-19 in the United States Using Topology and Machine Learning for Time Series Iryna Kotenko,
Kostiantyn Drach		 source
video
presentation source		 32
SGF 2020 Data Preparation Techniques for Cloud-Based Data Sources Jennifer L. Nenadic source 11
SGF 2020 Data Standardization Using SAS Health Data Mapper Eric Bolender source 14
PharmaSUG 2020 Analysis Package e-Submission - Planning and Execution Abhilash Chimbirithy,
Saigovind Chenna,
Majdoub Haloui		 source 8
PharmaSUG 2020 CDISC Standards for Medical Devices: Historical Perspective and Current Status Carey G. Smoak source 8
PharmaSUG 2020 Moving A Hybrid Organization Towards CDISC Standardization Kobie O'Brian,
Sara Shoemaker,
Robert Kleemann,
Kate Ostbye		 source 8
PHUSE US 2020 Automating the Analysis Data Reviewer's Guide (ADRG) in Early-stage Development Studies Jing Su,
Pranab K. Mitra		 source 5
PHUSE US 2020 Building a Deeper Bench: Writing ADaM Specifications Kristen Reece Harrington,
Shane Rosanbalm		 source
presentation source		 3
PHUSE US 2020 Data Standards for eCOA in Clinical Trials Terek Peterson,
Franklin E. Menius		 source
presentation source		 6
PHUSE US 2020 Data, Metadata and the notion of Holons* (* Information concepts) Peter Tormay source
presentation source		 7
PHUSE US 2020 Developing SEND for CBER - Collaborative Workstream Initiative Update Lisa Lin,
Susan DeHaven		 source
presentation source		 6
PHUSE US 2020 Implementing New Technical Guidance: A Sponsor Experience with the April 2018 CBER Vaccine Guidance Liping Zhang,
Sandra VanPelt Ngyuen		 source
presentation source		 8
PHUSE US 2020 Industry Experiences Submitting Standardized Study Data to Regulatory Authorities Janet Low,
Vincent Guo		 source
presentation source		 12
PHUSE US 2020 Let Us Trace Back to the Beginning from the End Madhusudhan Reddy Papasani,
Swathi Kotla		 source
presentation source		 12
PHUSE US 2020 Managing Simultaneous Drug Submissions with Breakthrough Designations - Lessons Learned from a Programming Perspective LiFeng Good source
presentation source		 6
PHUSE US 2020 Mind the Gap: Raw Data Model Julie Smiley source
presentation source		 7
PHUSE US 2020 Standards Compliance - An Automated Way to Measure the Interoperability of Clinical Studies Rammprasad Ganapathy source
presentation source		 6
PHUSE US 2020 Using Graph Technology for Metadata-driven Clinical Development Frederik Malfait source 6
PHUSE US 2020 What You Need to Know About Submitting Data to the FDA Pritesh Solanki,
Janet Low		 source
presentation source		 7
PHUSE EU 2019 Addressing the Gap in Data Standards: Introducing the Aggregation Layer Claudio Garutti,
Marko Bomyer		 source
presentation source		 11
PHUSE EU 2019 FAIR Data Standards in the GDSR Huw Mason source
poster source		 4
PHUSE EU 2019 Governance for Global Data QC Checks Kristien Nuyts source
presentation source		 10
PHUSE EU 2019 Navigating FDA Requirements: ISS/ISE Build Strategies Priyank Patel source 9
PHUSE EU 2019 Structured Clinical Development - Using a Digitized Study Design and Planning to Drive Process Automation Djenan Ganic source
presentation source		 7
MWSUG 2019 Abstracting and Automating Hierarchical Data Models: Leveraging the SAS FORMAT Procedure CNTLIN Option To Build Dynamic Formats That Clean, Convert, and Categorize Data Troy Martin Hughes 20
WUSS 2019 Stay Ahead of the Curve: How to implement New FDA Recommendation Study Data Standardization Plan (SDSP) in your organization? Stay Ahead,
Aakar Shah		 source 10
PharmaSUG 2019 Best Practices in Data Standards Governance Melissa R. Martinez source 4
PharmaSUG 2019 Designing Flexible Data Standards Models Melissa R. Martinez source 4
PharmaSUG 2019 Metadata Repository V1.0 - A Case Study in Standards Governance Aparna Venkataraman source 7
PharmaSUG 2019 PROC SQL to the Rescue: When a Data Step Just Won-t Do Anymore John R. O'Leary source 11
PharmaSUG 2019 SDSP (Study Data Standardization Plan) Case Studies and Considerations Kiran Kumar Kundarapu source 8
PharmaSUG 2019 Streamlining the Metadata Management Process Using SAS Life Science Analytics Framework Alex Ford source 6
PharmaSUG 2019 The Anatomy of Clinical Trials Data: A Beginner's Guide Venky Chakravarthy source 14
PharmaSUG 2019 The Need for Therapeutic Area User Guide Implementation Michael Beers source 8
SGF 2019 Data Modeling for a Better Analytical Environment Linus Hjorth source 12
SGF 2019 Zero-Inflated and Zero-Truncated Count Data Models with the NLMIXED Procedure Robin High source 18
PHUSE US 2019 A Linked Data Model and Hypermedia API for CDISC Share 2.0 Samuel Hume,
Frederik Malfait		 source 12
PHUSE US 2019 A Paradigm Shift to Represent and Manage Clinical Data Standards for Creating Data-driven Specification Veena Nataraj source
presentation source		 9
PHUSE US 2019 Best Practices in Data Standards Governance Melissa R. Martinez source
presentation source		 3
PHUSE US 2019 Building SQL Scripts Using Google Sheets R and R Shiny Huiming Tu source
presentation source		 19
PHUSE US 2019 Developing SEND for CBER - Collaborative Workstream Initiative Lisa Lin,
Susan DeHaven		 source
presentation source		 6
PHUSE US 2019 Developing, Implementing and Governing End-to-End Standards at Gilead Dhananjay Chhatre source
presentation source		 5
PHUSE US 2019 Evolving CDISC to the Next Decades: The CDISC Proof of Concept Peter Van Reusel,
Samuel Hume		 source
presentation source		 3
PHUSE US 2019 High-quality Study Data Standards for Submission Majdoub Haloui,
Ellen L. Asam		 source
presentation source		 9
PHUSE US 2019 Making the Case for Metadata Development Mike Molter source
presentation source		 7
PHUSE US 2019 Mapping Programs - Written by MDR Jörn Bilow source
presentation source		 2
PHUSE US 2019 Maximizing the Use of Patient Data Warehouse via Visual Analytics Sandy Lei,
Simon Alex		 source
presentation source		 7
PHUSE US 2019 Metadata-driven Automation in Drug Research Hanming Tu,
Zhongping Lin		 source
presentation source		 13
PHUSE US 2019 Next Generation Data Management: Case Studies for Ontology-driven Graph Databases Jim Lapointe source
presentation source		 8
PHUSE US 2019 SDSP (Study Data Standardization Plan) Case Studies and Considerations Kiran Kumar Kundarapu,
Nicole Gallegos		 source
poster source		 6
PHUSE US 2019 Striking a Balance: Adoption of Analysis Results Metadata (ARM) in Early Development Studies Janet Low,
Pranab K. Mitra		 source
presentation source		 6
PHUSE US 2019 The Need for Therapeutic Area User Guide Implementation Michael Beers source
presentation source		 7
PHUSE US 2019 What Does Good Look Like in the Study Data Standardization Plan (SDSP)? Pritesh Solanki,
Janet Low		 source
presentation source		 5
PHUSE EU 2018 Data Transparency - Breaking Down Data Silos for Improved Insight Peter Tormay,
Anna Berg		 source
presentation source		 8
PHUSE EU 2018 Diagnostics of technical errors in define.xml file Sergiy Sirichenko,
Max Kanevsky		 source
presentation source		 9
PHUSE EU 2018 Is it Possible to Make a Global CDISC Submission? Marianne Carames source
presentation source		 2
PHUSE EU 2018 Mapping Programs - Written by MDR Jörn Bilow source
presentation source		 2
PHUSE EU 2018 Top Five Challenges in Complying with CDISC Standards Trine Danø Klingberg,
Mikkel Traun		 source
presentation source		 4
PHUSE EU 2018 Use of HL7 FHIR as eSource to Pre-populate CDASH Case Report Forms Using a CDISC ODM API Samuel Hume,
Geoff Low		 source
presentation source		 12
SESUG 2018 Abstracting and Automating Hierarchical Data Models: Leveraging the SAS FORMAT Procedure CNTLIN Option To Build Dynamic Formats That Clean, Convert, and Categorize Data Troy Martin Hughes source 20
WUSS 2018 Abstracting and Automating Hierarchical Data Models: Leveraging the SAS FORMAT Procedure CNTLIN Option To Build Dynamic Formats That Clean, Convert, and Categorize Data Troy Martin Hughes source 21
PHUSE US 2018 A Successful Meta-Data Repository (MDR): It's About Managing Relationships Philip Giangiulio,
Melanie A. Paules		 source
presentation source		 7
PHUSE US 2018 Automate Analysis Result Metadata in the Define-XML v2.0 Hong Qi,
Larry Wu		 source
presentation source		 8
PHUSE US 2018 Challenges and Tactics of Managing Clinical Programming in Long Term Outcomes Trials David L. Wade,
Joanne C. Zhou,
Rakesh Kumar		 source
presentation source		 6
PHUSE US 2018 Commissioning a MDR System: Next-generation of Standards implementation Abhinav Jain source
presentation source		 6
PHUSE US 2018 Comparing and Contrasting Differences between the PHUSE SDSP and CBER Checklist Janet Low,
Pritesh Solanki		 source
presentation source		 5
PHUSE US 2018 FDA CBER Data Standards Activity Update Lisa Lin source
presentation source		 4
PHUSE US 2018 FDA View: Technical Rejection Criteria for Study Data Ethan Chen,
Lilliam Rosario		 source
presentation source		 4
PHUSE US 2018 How to Prepare High Quality Metadata for Submission [presentation] Varun Debbeti source 31
PHUSE US 2018 Machine Learning Driven Clinical Insights - What When & How? [presentation] Chandi Kodthiwada source 5
PHUSE US 2018 Making PK Analysis Easier: The New ADaM Data Standard ADNCA Peter Schaefer source
presentation source		 6
PHUSE US 2018 Ready Set Go: Planning and Preparing a CDISC Submission Maria Dalton source
presentation source		 11
PHUSE US 2018 Role of Associate Director of Biomedical Informatics in Clinical Review at the FDA Nhi Beasley source 2
PHUSE US 2018 SDTM and SEND: An Integrated View and Approach Veena Nataraj,
Cheryl Riel		 source
presentation source		 11
PHUSE US 2018 Use of HL7 FHIR as eSource to Pre-populate CDASH Case Report Forms Using a CDISC ODM API Samuel Hume,
Geoff Low		 source
presentation source		 12
PharmaSUG 2018 A Framework for Implementing [Conflicting] FDA Guidance Todd Case source 6
PharmaSUG 2018 Automating and Abstracting SAS Format Creation: Leveraging the CNTLIN Option To Build Dynamic SAS Formats That Clean, Convert, and Categorize Data Troy Martin Hughes source 21
PharmaSUG 2018 Avoid chasing one's Tail - Challenges and Solutions for managing changes in SDTM Standards Development Erica Davis,
Veena Nataraj		 source 7
PharmaSUG 2018 Best Practices in Data Standards Governance Melissa R. Martinez source 4
PharmaSUG 2018 Complying with the ADaM Compliance Rules Alyssa M. Wittle,
Steven R. Kirby		 source 4
PharmaSUG 2018 Data Standards for Population Pharmacokinetic (POPPK) and Non-Compartmental Analysis (NCA) Neelima Thanneer source 7
PharmaSUG 2018 Designing Flexible Data Standards Models Melissa R. Martinez source 4
PharmaSUG 2018 Diagnostics of technical errors in define.xml file Sergiy Sirichenko,
Max Kanevsky		 source 9
PharmaSUG 2018 Electronic Data Submission and Utilization in Japan Yuki Ando source 25
PharmaSUG 2018 How PK and PD analyses drive dataset designs David Radtke,
Brian A. Moser		 source 7
PharmaSUG 2018 Leveraging Standards for Effective Visualization of Early Efficacy in Clinical Trial Oncology Studies Kelci J. Miclaus,
Lili Li		 source 12
PharmaSUG 2018 Why organizations need MDR systems to manage metadata? Abhinav Jain source 7
SGF 2018 Alternative Variance Parameterizations in Count Data Models Robin High source 14
SGF 2018 The Anatomy of Clinical Trials Data: A Beginner's Guide Venky Chakravarthy source 14
PHUSE EU 2017 Ahead of the Curve: Leading with Industry Data Requirements Nancy Haeusser source
presentation source		 8
PHUSE EU 2017 Applying the OMOPCommon Data Model to Dutch Healthcare Data: A Case Study Rients van Wijngaarden source
presentation source		 5
PHUSE EU 2017 Career Development Through Job Rotation: Cases and Lessons Learned Simon Wang source
presentation source		 2
PHUSE EU 2017 CDISC Transport Standards - A Glance Edwin Ponraj Thangarajan,
Giri Balasubramanian		 source
presentation source		 14
PHUSE EU 2017 Clinical Metadata - Web-based metadata management with a CDISC mindset Andrew Ndikom,
Liang Wang		 source
presentation source		 12
PHUSE EU 2017 Clinical Study Oversight: Different Approaches to Using Data Standards Jasmine Kestermont,
Peter Van Reusel		 source
presentation source		 6
PHUSE EU 2017 Cross Functional Standards Governance for Pharma Warwick Benger source
presentation source		 6
PHUSE EU 2017 Cross Functional Standards Governance for Pharma Sheetal Patel,
Warwick Benger		 source
presentation source		 6
PHUSE EU 2017 Harmonizing SDTM at the Source: Designing Collection Instruments that Support Sponsor Standards Sue Huxtable,
Charlotte Lomberg		 source
presentation source		 7
PHUSE EU 2017 How a Metadata Repository can Facilitate Automated Data Collection Processes Judith Goud source
presentation source		 8
PharmaSUG 2017 A Precision-strike Approach to Submission Readiness: How to Prepare Your Filing Teams for Consistent Excellence Michael Hagendoorn,
Tony Chang		 source 7
PharmaSUG 2017 Ahead of the Curve: Leading with Industry Data Requirements Maria Dalton,
Nancy Haeusser		 source 17
PharmaSUG 2017 Gray Areas of ADaM and Ways to Provide Color [presentation] Susan J. Kenny,
Sandra Minjoe,
Nate Freimark,
Jack Shostak,
John K. Troxell,
Deborah J. Bauer		 source 38
PharmaSUG 2017 Quality Check your CDISC Data Submission Folder Before It Is Too Late! Bhavin Busa source 9
PharmaSUG 2017 Tips and Best Practices using SAS Analytics Tho H. Nguyen,
Paul Segal		 source 7
SGF 2017 Develop a Simple Data Governance Program for a SAS Customer Intelligence Environment in 90 Days Aaron Nelson source 12
SGF 2017 Implementing Role-Based Access Control and DSoD Authorization Schema on SAS Perttu Muurimaki source 15
SGF 2017 Investigating Connections between Disparate Data Sources with SAS Visual Investigator Gordon Robinson source 10
SESUG 2016 Predicting student success based on interactions with virtual learning environment Vivek Doijode,
Neha Singh		 source 10
PHUSE EU 2016 Data Standards Governance João Gonçalves source
presentation source		 6
PHUSE EU 2016 Effective Use of a Metadata Repository Across Data Operations: The Need for a Machine Readable Form Isabelle de Zegher,
Michele Gray,
Mark Sullivan,
Michael Goedde		 source
presentation source		 5
PHUSE EU 2016 Efficiency comes From Reusability and Repeatability Hanming Tu,
Dave Evans		 source
presentation source		 10
PHUSE EU 2016 Pattern-based MDR: Towards High-quality Data Standards Alan Cantrell,
Julius Kusserow		 source
presentation source		 7
PHUSE EU 2016 Planning for Data Reporting Processes for Submission: Key Considerations Parag Shiralkar source
presentation source		 2
PHUSE EU 2016 Reflect on Your Data Peter Tormay,
Henrik Drews		 source
presentation source		 9
PHUSE EU 2016 The Playbook: Real-world Data to Real-world Intelligence Laurie Rose,
S. Robert Collins		 source
presentation source		 7
PHUSE EU 2016 To Create Define-XML Using - XML and the OpenCDISC Validator [presentation] Murali Neela source 17
PHUSE EU 2016 Understanding the Potential of Share: A Visual Business Case and Technical Use Case Peter Van Reusel source
presentation source		 4
PharmaSUG 2016 Achieving Clarity through Proper Study Documentation: An Introduction to the Study Data Reviewer's Guide (SDRG) Michael Stackhouse,
Terek J. Peterson		 source 5
PharmaSUG 2016 Preparing Legacy Format Data for Submission to the FDA - When & Why Must I Do It, What Guidance Should I Follow? David C. Izard source 11
PharmaSUG 2016 Submission-Ready Define.xml Files Using SAS Clinical Data Integration Melissa R. Martinez source 10
SGF 2016 SAS Customer Intelligence 360: Creating a Consistent Customer Experience in an Omni-channel Environment Mark Brown,
Brian Chick		 source 16
PHUSE EU 2015 A Model for Reviewing the Operational Implementation of the CDISC Standards Andy Richardson source
presentation source		 7
PHUSE EU 2015 Data-centric System Development Life Cycle for Automated Clinical Data Development Systems Kevin Lee source
presentation source		 5
PHUSE EU 2015 E2E Data Standards: The Need for a New Generation of Metadata Repositories Isabelle de Zegher source
presentation source		 4
PHUSE EU 2015 FDA Review Principles Applied to CRO Oversight Sascha Ahrweiler,
Grace Ignacio		 source
presentation source		 7
PHUSE EU 2015 From Data to Knowledge: Semantics and Implementations Judith Goud,
Julie Smiley		 source
presentation source		 5
PHUSE EU 2015 Understanding SE, TA, TE Domains Jacques Lanoue source
presentation source		 4
PharmaSUG CN 2015 Reading and Resolving OpenCIDSC Message [presentation] Yu Pang 23
PharmaSUG 2015 Begin with the End in Mind - Using FDA Guidance Documents as Guideposts when Planning, Delivering and Archiving Clinical Trials David C. Izard source 12
PharmaSUG 2015 Managing Custom Data Standards in SAS Clinical Data Integration Melissa R. Martinez source 17
PharmaSUG 2015 PhUSE De-Identification Working Group: Providing De-Identification Standards to CDISC Data Models Jean-Marc Ferran,
Jacques Lanoue		 source 8
PharmaSUG 2015 Understanding SE, TA, TE Domains Jacques Lanoue source 4
PharmaSUG 2015 Using SAS Clinical Data Integration to Roundtrip a Complete Study Study Metadata (Define-XML) and Study Data (Dataset-XML) Ken Ellis source 19
SGF 2015 SASTRACE: Your Key to RDBMS Empowerment Andrew Howell source 12
SGF 2015 The Business of Campaign Response Tracking Pamela Dixon source 8
PHUSE EU 2014 ADaM Standards: What's New? Gavin Winpenny source
presentation source		 9
PHUSE EU 2014 CDISC Dataset-XML - A Dataset Structure for Clinical Trial Data Transport for Future Drug Submissions Joerg Dillert source
presentation source		 6
PHUSE EU 2014 Change Management - An ICON Approach and Case Study Anagha Pradhan source
presentation source		 4
PHUSE EU 2014 Clinical Study Data Processes @ LEO Pharma Joergen Iversen source
presentation source		 4
PHUSE EU 2014 Data Transparency through Metatada Management Judith Goud,
Julie Smiley		 source
presentation source		 4
PHUSE EU 2014 Data Transparency: Data De-identification and the Role of the Programmer [presentation] Jean-Marc Ferran source 20
PHUSE EU 2014 Every Study is Special! - Governing Data Standards Chris Price,
Elizabeth Nicol		 source
presentation source		 12
PHUSE EU 2014 FDA Guidance on Standardised Study Data for Electronics Submissions Lauren L. Shinaberry,
Éanna Kiely		 source
presentation source		 7
PHUSE EU 2014 Is Your Clinical Data Standards Library Ready for Change? Adapting to TA Specific Standards Lauren L. Shinaberry source
presentation source		 6
PHUSE EU 2014 Metadata, Study Standards, Interoperability: Key Concepts Toward Compliance to FDA Guidance Isabelle de Zegher source
presentation source		 3
PHUSE EU 2014 Models, Metadata and Messaging: Exploring Standards Governance in the CDISC Era Kenneth Stoltzfus source
presentation source		 6
PHUSE EU 2014 Representation of CDISC Foundational Standards Using RDF Authors Scott A. Bahlavooni,
Frederik Malfait		 source
presentation source		 3
PHUSE EU 2014 Spotfire for Clinical and Translational Medicine Gerard Conway source 3
PHUSE EU 2014 Standards Driven Innovation [presentation] Frederik Malfait source 36
PHUSE EU 2014 The Capish Information Model - Simplify Access to Your Data Anna Berg,
Catharina Dahlbo		 source
presentation source		 8
PHUSE EU 2014 The PHUSE Therapeutic Area Wiki Page Jothy Kalathiparampil,
Oliver Wirtz		 source
presentation source		 2
PHUSE EU 2014 Update on Regulatory Guidance: Data Standardisation Planning for Clinical Development Programs James R. Johnson source
presentation source		 10
MWSUG 2014 SAS In-Memory Analytics: Beyond Foundation SAS Tho H. Nguyen,
John Cunningham		 4
WUSS 2014 SAS In-Memory Analytics: Beyond Foundation SAS John Cunningham,
Tho H. Nguyen		 source 4
PharmaSUG 2014 A Road Map to Successful CDISC ADaM Submission to FDA: Guidelines, Best Practices & Case Studies Vikash Jain,
Sandra Minjoe		 source 9
PharmaSUG 2014 Adopted Changes for SDTMIG v3.1.3 and 2013 OpenCDISC Upgrades Yi Liu,
Stephen Read		 source 17
PharmaSUG 2014 Clinical Trial Data Integration: The Strategy, Benefits, and Logistics of Integrating Across a Compound Natalie Reynolds,
Keith Hibbetts		 source 12
PharmaSUG 2014 Data Standards Development for Therapeutic Areas: A Focus on SDTM-Based Datasets Fred Wood,
Diane Wold,
Rhonda Facile,
Wayne Kubick		 source 10
PharmaSUG 2014 Forging New SDTM Standards for In-Vitro Diagnostic (IVD) Devices: A Use-Case Carey G. Smoak,
Smitha Krishnamurthy,
Mansi Singh,
Sy J. Truong		 source 6
SGF 2014 CMS Core Measures, the Affordable Care Act, and SAS Visual Analytics Joe Whitehurst,
Diane Hatcher		 source 16
SGF 2014 Integrating and Using Hierarchical Vocabularies in SAS Glenn Colby source 22
PHUSE EU 2013 Going Against the Flow: Backmapping SDTM Data Panteleo Nacci source
presentation source		 7
PHUSE EU 2013 Is your Library a Success: Manage & Measure Conformance Across Partners and Projects Lauren L. Shinaberry,
Bart Van Win		 source
presentation source		 4
PHUSE EU 2013 Leading a Team When you are Note the Subject Matter Expert Vijay Reddi source
presentation source		 8
PHUSE EU 2013 Semantic Technology and CDISC Standards Frederik Malfait,
Scott A. Bahlavooni		 source
presentation source		 13
PHUSE EU 2013 Standards for the Management of Clinical Trial Data, Why are they Needed, What is Needed? Isabelle Abousahl source
presentation source		 11
PHUSE EU 2013 Standards Governance - A First Insight Claudia Meurer source
presentation source		 6
PHUSE EU 2013 The Evolution of SDTM - What's New Tina Apers source
presentation source		 5
PHUSE EU 2013 Time Travel for Librarians: Versioning Complex Library Metadata for Past, Present or Future Retrieval Nico De Leeuw,
Ine Felsenstein		 source
presentation source		 12
NESUG 2013 Pooling strategy for clinical data Abraham Yeh,
ShinRu Wang,
Xiaohong Zhang		 11
PharmaSUG 2013 From Standards that Cost To Standards that Save: Cost Effective Standards Implementation Jeffrey M. Abolafia,
Frank C. DiIorio		 source 9
PharmaSUG 2013 Getting Ready for PDUFA V - The New "GCP": Governance, Communication, Planning Joanna Koft source 5
PharmaSUG 2013 Introduction to the CDISC Standards Sandra Minjoe source 10
PharmaSUG 2013 Life Cycle of a Data Point - A Tool to Educate the Clinical Development Team on What it Takes to Go From the Clinic to a Submission Arthur Collins,
Joanna Koft		 source 4
PharmaSUG 2013 Map Metadata - Going Beyond the Obvious/Connecting the Dots Gregory C. Steffens,
Praveen Garg		 source 8
PharmaSUG 2013 OpenCDISC: Beyond Point and Click Frank C. DiIorio source 12
PharmaSUG 2013 Standardizing the Standards: A Road Map for Establishing, Implementing and Unifying Standards in Your Organization Amy Caison,
Jhelum Naik,
Tammy Jackson		 source 9
SGF 2013 Fueling the Future of an Energy Company Stijn Vanderlooy source 11
SGF 2013 Hot off the Press: SAS Marketing Automation 6.1 Brian Chick,
Mark Brown		 source 16
SGF 2013 Using SAS to Dynamically Generate SAS Code in Order to Display Both Variable Label and Name as Column Header in PROC REPORT and PROC PRINT Heli Ghandehari,
Victor Lopez		 source 5
NESUG 2012 Length of Intensive Care Unit Stay Computed from the VA Corporate Data Warehouse Adeline J. Wilcox 14
PHUSE EU 2012 Mapping the Company's Legacy Data Model to SDTM Anja Feuerbacher,
Bruce Rogers		 source
presentation source		 7
PHUSE EU 2012 One Approach to a Metadata and Data Standards Repository Bill J. Gibson source
poster source		 4
PHUSE EU 2012 Using Metadata to Integrate and Standardise Clinical Trial Data - the ICON Study Data Mapper Paul Crean,
Jennie McGuirk		 source
presentation source		 6
SESUG 2012 An Introduction to the Clinical Standards Toolkit Mike Molter source 13
SESUG 2012 SAS Programming tips and techniques for Data Mapping Sheetal Nisal source 7
PharmaSUG 2012 An Introduction to the Clinical Standards Toolkit and Clinical Data Compliance Checking Mike Molter source 14
PharmaSUG 2012 Experiences in Leading a Company-Wide First CDISC Filing from a Programming Perspective Sho-Rong Lee source 6
SGF 2012 Beyond Star Schema: Exploring the Next Query Generation with the SAS Enterprise BI Server Fred Levine source 6
SGF 2012 Defining the Development Process and Governance of Implementing ADaM within an Organization Chris Decker source 11
SGF 2012 Developing Custom Metadata Reports for SAS Data Integration Studio Michael Kilhullen source 12
SGF 2012 How Does SAS In-Database Analytics Impact Data Management? Adrian Jones source 8
SGF 2012 Using Custom Data Standards in SAS Clinical Data Integration Michael Kilhullen source 11
SESUG 2011 Proc CDISC: Implementation and Assessments Sheetal Nisal source 6
PHUSE EU 2011 Creating ADaM Friendly Analysis Data from SDTM Using Meta Data Erik Brun,
Rico Schiller		 source
presentation source		 6
PHUSE EU 2011 Defining the Governance and Process of Implementing ADaM across an Organization Chris Decker source
presentation source		 11
PHUSE EU 2011 Implementing ADaM Using the SAS Clinical Standards Toolkit Gene Lightfoot source
presentation source		 12
PHUSE EU 2011 SAS Drug Development as a platform governing data standards specification and clinical data exchange between pharmaceutical organizations Tina Apers source
presentation source		 56
MWSUG 2011 Driving Clinical Safety Reviews with Data Standards Geoffrey A. Mann 7
SGF 2011 Base SAS Methods for Building Dimensional Data Models Christopher W. Schacherer source 12
SGF 2011 Driving Clinical Safety Reviews with Data Standards Geoffrey A. Mann source 7
SGF 2011 How TV 2 Improves Data Quality and Facilitates a Unified Customer View for Optimizing the Customer Experience Svein O. Gundhus,
Terje Vatle		 source 12
SGF 2011 PROC PANEL Vs. A FAST ALGORITHM FOR ESTIMATION OF UNBALANCED PANEL DATA MODELS WITH TWO FIXED EFFECTS Alan Ricardo da Silva,
Mariana Fernandes Teixeira,
Thaís Helena Fernandes Teixeira		 source 12
SGF 2011 State of the Union: The Crossroads of CDISC Standards and SAS Supporting Role Michael J. Molter,
Chris Decker		 source 14
NESUG 2010 The Past, Present, and Future of Clinical Data Standards Chris Decker 10
PHUSE EU 2010 AstraZENeca and the ART of metadata maintenance Paul Frost source
presentation source		 11
PHUSE EU 2010 Bridging the communication gap: implementing metadata standards in trial protocols Annabel Acs source
presentation source		 7
PHUSE EU 2010 Challenges of Clinical projects shared between Pharma Companies [presentation] Oliver LeConte source 27
PHUSE EU 2010 Define.xml - Tips and Techniques for Creating CRT-DDS Julie A. Maddox,
Mark Lambrecht		 source
presentation source		 10
PHUSE EU 2010 From Data Capture to Decision Making Innovation through Standardization Michaela Jahn,
Stephan Laage-Witt		 source 5
PHUSE EU 2010 Introduction to SAS Clinical Standards Toolkit Andreas Mangold,
Nicole Waechter		 source
presentation source		 16
PHUSE EU 2010 The Use of Meta Data in Creating, Transforming and Transporting Clinical Data Gregory C. Steffens source
presentation source		 9
PharmaSUG 2010 Accessing and using the metadata from the define.xml Lex Jansen 22
PharmaSUG 2010 Accessing and using the metadata from the define.xml [presentation] Lex Jansen 74
PharmaSUG 2010 Managing Clinical Data Standards: An Introduction to SAS Clinical Data Integration Michael Kilhullen 10
PharmaSUG 2010 Quality in a World of "Standards" with Differences! Sandra VanPelt Nguyen 9
PharmaSUG 2010 Thanks CDISC - Free Utilities Robert Agostinelli 5
SGF 2010 Business Intelligence Solution to Improve Educational Standards and Performance for an Australian State Education Authority Gurupratap S. Dsor source 4
SGF 2010 Managing Clinical Data Standards: An Introduction to SAS Clinical Data Integration Michael Kilhullen source 10
SGF 2010 So You Need a Data Warehouse But Don't Have the Budget to Build One: What Now? Steve Morton source 11
SGF 2010 Tabular Reporting Data Standard Frederick A. Cieri source 9
SGF 2010 The Past, Present, and Future of Clinical Data Standards Chris Decker source 10
SGF 2010 Understanding the define.xml File and Converting It to a Relational Database Lex Jansen source 20
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 DI Studio - will we need new MetaProgrammers? Simon Wilcock,
Sireesha Potula		 source
presentation source		 11
PHUSE EU 2009 ETL and the Clinical Programmer - They don't have to be Enemies! Chris Decker,
Christopher R. Olinger		 source 11
PHUSE EU 2009 SDTM Validation: How can we do it right? Peter Van Reusel source
presentation source		 8
PHUSE EU 2009 Using SAS Clinical Data Integration Server to Implement and Manage CDISC Standards Julie A. Maddox source
presentation source		 8
NESUG 2009 Deciding if the EM Algorithm is the Right Choice Michael B. Moldoff 3
WUSS 2009 The Second CDISC Pilot Project: A Metastandard for Integrating Databases Gregory C. Steffens,
Ian Fleming		 source 5
PharmaSUG 2009 Converting the define.xml to a Relational Database to Enable Printing and Validation [presentation] Lex Jansen 76
PharmaSUG 2009 RS01 The Second CDISC Pilot Project A Metastandard for Integrating Databases Gregory C. Steffens 4
SGF 2009 Implementing CDISC When You Already Have Standards: A Case Study Sandra Minjoe source 10
SGF 2009 The Second CDISC Pilot Project: Standards for Integrating Databases Ian Fleming,
Gregory C. Steffens		 source 4
SGF 2009 Using SAS Clinical Data Integration Server to Implement and Manage CDISC Standards Michael Kilhullen source 7
PHUSE EU 2008 CDISC Implementation Strategies: Exploit your data assets while still giving the FDA what they want David Smith source 9
PHUSE EU 2008 Implementing CDISC at Boehringer Ingelheim Michael Knoessl,
Peter Leister		 source 5
PharmaSUG 2008 Cost-Effective Solution to Automating the Creation of CDISC define.xml: Using SAS Data _Null_ with Relational Data Model via SAS/AF Application Annie S. Guo 12
PharmaSUG 2008 SDTM, Plus or Minus Barry R. Cohen 6
SGF 2008 Modeling Zero-Inflated Count Data with Underdispersion and Overdispersion Adrienne Tin source 11
WUSS 2007 RDBMS Setup and Authentication in SAS 9 Paresh M. Patel,
Richard Kerwin		 source 9
PHUSE EU 2007 All roads lead to SDTM - which one shall we take? Ian Fisher,
Donna Thompson		 source 9
PharmaSUG 2007 CDISC Implementation Step by Step: A Real World Example Sy J. Truong 19
PharmaSUG 2007 SDTM, Plus or Minus Barry R. Cohen 6
PharmaSUG 2007 The Submission Data File System Automating the Creation of CDISC SDTM and ADaM Datasets Marcus Bloom,
David Edwards		 15
PharmaSUG 2007 The Use of CDISC Standards in SAS from Data Capture to Reporting Andrew T. Fagan 21
PNWSUG 2006 Advanced Warehousing with SAS9 Gary Mehler 17
PHUSE EU 2006 Contours of a Drug Development Data Warehouse Paul Vervuren source 8
PHUSE EU 2006 The Submission Data File System Automating the Creation of CDISC SDTM and ADaM Datasets David Edwards,
Marcus Bloom		 source 6
PHUSE EU 2006 The Use of CDISC Standards in SAS from Data Capture to Reporting Andrew T. Fagan source 21
SESUG 2006 Stars and Models: How to Build and Maintain Star Schemas Using SAS Data Integration Server in SAS9 Nancy A. Rausch source 24
WUSS 2006 Advanced Warehousing with SAS9 Gary Mehler source 17
NESUG 2006 Using SAS Data Integration Studio to Convert Clinical Trials Data to the CDISC SDTM Standard Barry R. Cohen 8
PharmaSUG 2006 Using SAS ETL Studio to Convert Clinical Trials Data to the CDISC SDTM Barry R. Cohen 10
SUGI 2006 Advanced Warehousing with SAS9 Gary Mehler source 17
SUGI 2006 Hiding the Complexity: A Customized Application for Accessing Multidimensional Data Phil Rhodes source 7
SUGI 2006 SAS/OR - Making Sense of Network Data with Network Visualization Workshop Edward P. Hughes,
Phil Meanor		 source 20
SUGI 2006 Stars and Models - How to Build and Maintain Star Schemas Using SAS ETL Server Nancy A. Rausch source 24
PHUSE EU 2005 Best Practices for Managing Clinical Research Information David Handelsman source 16
WUSS 2005 Data Integrity through DEFINE.PDF and DEFINE.XML Sy J. Truong source 14
WUSS 2005 Transforming Data for CDISC and ISS Sy J. Truong source 11
PharmaSUG 2005 Pharmacovigilance and Drug Safety Reporting Algorithms (Content and Process) David Olaleye,
Michael Kilhullen,
Gail Kongable,
Tanyss Mason,
Eugenia Bastos,
Edward D. Helton		 8
SUGI 2005 Implementing Data Warehousing and Business Intelligence at McMaster University Using the SAS Intelligence Value Chain Debbie Weisensee,
Eric Matthews,
Anne McInnis		 source 10
SUGI 2005 PreMIS: Pre-hospital Medical Information System Jeff Wright,
Patrick H. Alston,
Sharon Schiro,
Tim Walters		 source 12
WUSS 2004 The Path to Data Standards Sy J. Truong source 10
PharmaSUG 2004 Data Standards with and without CDISC Sy J. Truong 8
PharmaSUG 2004 Tools to Facilitate the Creation of Pooled Clinical Trials Databases Patricia Majcher 8
WUSS 2003 Snapshots from Hell: Practical Issues in Data Warehousing Tyson Lee source 5
WUSS 2003 Using Graph-N-Go To Easily Present Your Data And Webenable Your Graphs Curtis A. Smith source 8
SESUG 2003 New Technologies for Delivering Data to Internal and External Clients Sigurd W. Hermansen source 5
SEUGI 2003 AstraZeneca Data Migration Project [presentation] David Smith,
Paul Frost		 source 39
SEUGI 2003 Business Intelligence with SAS 9.1 [presentation] Mark Torr source 31
SEUGI 2003 Intelligent Storage [presentation] Ingo Brenckmann source 19
SEUGI 2003 SAS ETL Studio @ work [presentation] Wilbram Hazejager source 26
SEUGI 2003 Second-generation data warehouse - strategic and tactics at the Vilnius Bank [presentation] Laukai source 22
SEUGI 2003 SPDE engine usage made easy with the SAS 9.1 metadata architecture [presentation] Jochen Kirsten source 99
PharmaSUG 2003 Clinical Data Model and FDA/CDISC Submissions Mark Edwards,
Gajanan Bhat		 10
PharmaSUG 2003 Clinical Data Standards - An eSubmissions Perspective Shy Kumar 6
PharmaSUG 2003 Standardizing Data Processing and e-Publishing for the Pharmaceutical Industry Shawn Wang 6
PharmaSUG 2003 StARScope: A Web-Based SAS Prototype for Clinical Data Visualization Fang Dong,
Subrahmanyam Pilli,
Scott Pivirotto,
Jeff Van Domelen		 6
SUGI 2003 New Technologies for Delivering Data to Internal and External Clients Sigurd W. Hermansen source 5
SUGI 2003 StARScope: A Web-Based SAS Prototype for Clinical Data Visualization Fang Dong,
Thomas Pivirotto,
Subrahmanyam Pilli,
Jeffrey L. Van Domelen		 source
MWSUG 2002 V9 OLAP - An Architectural Overview Duane E. Ressler 5
WUSS 2002 Generation of a Clinical Data Warehouse across Multiple Companies Sarbjit Rai source 4
SEUGI 2002 SAS and the CRO [presentation] Peter Stagg source 14
SEUGI 2002 The SAS Enterprise Architecture - Achieving Enterprise Integration [presentation] Paul Padley source 48
PharmaSUG 2002 Implementing a Standardized Data Model - A Real Life Experience Curtis Wolf,
Paul M. Gilbert		 4
PharmaSUG 2002 The CDISC Laboratory Data Interchange Standard: Using SAS To Read and Write CDISC Compliant Data Sets and Files Margaret Hung 8
SUGI 2002 Data Warehousing for the Enterprise Gary Mehler source 8
SUGI 2002 Unit-of-Analysis Programming Vanessa C. Hayden source 6
SUGI 2002 V9 OLAP - An Architectural Overview Duane E. Ressler source 5
MWSUG 2001 Parsing a SAS Database for Correctness: A Conceptual Introduction Edward F. Brown 8
VIEWS 2001 Managing Supplier Relationships In The E-World: The Need For Information [presentation] Jennifer Major,
Trevor Payne		 59
SESUG 2001 OLAP Best Practices - What You Need to Consider When Building and Deploying an OLAP Application Greg Henderson source 7
SEUGI 2001 Customer Profiling System in Telecom Italia Mobile [presentation] Claudio Bocci,
Gianni Santerini		 source 44
SEUGI 2001 Data Warehouse and Strategic Management - How to Sustain Competitive Advantage [presentation] Karin Nischk,
Wolfgang Hofbauer		 source 31
SEUGI 2001 Data Warehouse Technology As The Main Building Block of the Modern IT Strategy of the Polish Customs Adminstration [presentation] Andrzej Tyrowicz source 34
SEUGI 2001 Dynamic Budgeting & Plannin [presentation] Peter Bull source 33
SEUGI 2001 How To Find Your Way Around A Customer Database [presentation] Alberto Saccardi,
Fabio Marchetti		 source 24
SEUGI 2001 Multi-objective modelling of decision making problems using SAS software [presentation] J. Pietrzykowski,
J. Granat,
P. Witan		 source 30
PharmaSUG 2001 Compass: a web interface to a Data Warehouse for Pharmaceutical Decision Support Christine Vander Vorst 2
PharmaSUG 2001 The Changing Nature of SAS Programming in the Pharmaceuticals Industry Steven Light 4
PharmaSUG 2001 Unit-of-Analysis Programming Vanessa C. Hayden,
Fidelity Investments		 6
SUGI 2001 Building an Integrated Informational Backplane Mark Moorman source 7
SUGI 2001 Data Modeling in Clinical Data Analysis Projects Gajanan Bhat source 6
SUGI 2001 Using Graph-N-Go with ODS to Easily Present Your Data and Web-Enable Your Graphs Curtis A. Smith source 8
SESUG 2000 Implementing a balanced scorecard solution on top of SAP, using CFO vision as interface Ida Carpelle source 6
SESUG 2000 Think Thin 2-D: "Reduced Structure" Database Architecture Sigurd W. Hermansen source 5
SEUGI 2000 An online Business Monitoring System - Actual online information on highly automated Business Processes in a large scale SAP Environment - Case Study and Outlook [presentation] Elmar Husmann source 20
SEUGI 2000 From Doctor Shopping to Data Warehouseing to Improve Health Outcomes [presentation] John Trabinger source 47
SEUGI 2000 From the client datamart to the corporate data warehouse [presentation] Daniel Csikos source 19
SEUGI 2000 HR Vision for R/3 & HR knowledge solution [presentation] Dave Prinsloo source 44
SEUGI 2000 Implementing a Balanced Scorecard on top of SAP/RE-FI Using SAS CFO Vision as Interface [presentation] Ida R. Carapelle,
Sophie De Baets		 source 42
SEUGI 2000 Publitalia '80 Prj. MAGIA - global management of accounting collections [presentation] Antonio Bellato source 28
SEUGI 2000 Risk Dimensions V3 Overview [presentation] Rik van de Weerthof source 28
SEUGI 2000 SAS environment harnessed to reporting system execution at the customs distributed structure [presentation] Tadeusz Lewandowski,
Wojciech Bułakowski		 source 50
SEUGI 2000 The power of HOLAP in a multidimensional world [presentation] Massimo Martucci source 42
SUGI 2000 An Application for the Analysis and Visualization of Disease Incidence Data Paul Nicholson,
Deborah Allon,
Estelle A. Gilman		 source 9
NESUG 1999 Understanding Behavioral Trends and Patterns in Populations: Revisiting the Clinical Pathway Model Enya N. B. Garcia 1
SEUGI 1999 An application for the analysis and visualisation of disease incidence data Deborah Allon,
Estelle Gilman,
Paul Nicholson		 source 9
SEUGI 1999 Exploiting data warehouse metadata for knowledge management [presentation] Berthold Weismann source 27
SEUGI 1999 Intranet-based applications in Bank Handlowy [presentation] Zdzisław Dec source 23
SEUGI 1999 Star's the limit.Ad hoc, cross-subject queries with the SAS system in a dimensional data warehouse [presentation] Wojciech Chybowski source 30
SEUGI 1999 Supply chain management a new challenge for SAS data warehousing [presentation] Pascal de Poorter source 33
SUGI 1999 Relational Database Schemes and SAS Software SQL Solutions Sigurd W. Hermansen source 9
SUGI 1999 The Quality Data Warehouse - Solving Problems for the Enterprise Brad Klenz,
Donna O. Fulenwider		 source 8
SEUGI 1998 Database marketing applications in the Italian banking sector Alberto Saccardi,
Guido Cuzzocrea		 source 8
SEUGI 1998 Installation of an MIS and data warehouse in Bank Handlowy in Warsaw: Business Benefits Zdzisław Dec source 8
SEUGI 1998 Reporting system for a commercial bank: A case study Tadeusz Stawicki source 6
SEUGI 1998 Using SAS Software as a decision support system on top of the R/3 System FI financial accounting module Ida R. Carapelle source 14
PharmaSUG 1998 Managing SAS/PH-Clinical in a Multiple Instance Environment Steven Light,
Paul M. Gilbert		 3
SUGI 1998 Building the Framework for Enterprise Data Analysis in the Semiconductor Industry John T. Stokes,
Roger Thompson		 source 6
SEUGI 1997 Data Modelling for an epidemiological database Deborah Allon,
Paul Nicholson		 source 11
SEUGI 1997 Implementation of data warehouse and reporting at Fokus Bank Håvar Wold source 14
SCSUG 1996 The SAS System in a Data Warehouse Environment T. Randall Betancourt 12
SESUG 1996 The SAS System in a Data Warehouse Environment T. Randall Betancourt 12
MWSUG 1996 The SAS System in a Data Warehouse Environment T. Randall Betancourt 12
SEUGI 1996 Building an efficient data warehouse: understanding the issues of data summarization and ... Scott Anderson source 52
SEUGI 1996 Data Warehousing Sean Kelly source 31
SEUGI 1996 MUDIS - a front ending multidimensional data exploitation application Fritz Ederer source 7
SEUGI 1996 Re-engineering the BBL Data Warehouse Claude Baillieux source 37
SUGI 1996 Extending SAS/EIS Software Ann Weinberger source 7
SUGI 1996 RAD with SAS Software: Strategies, Techniques, and TipS Samuel Berestizhevsky,
Tanya Kolosova		 source 6
SEUGI 1995 UBIRIS - A System to Support Investment Research and Publications at UBS Beat Moser source 10
MWSUG 1994 Access Control Mechanism in Behaviorally Object-Oriented Databases Cristian Radu,
Mark Vandenwauver,
Rene Govaerts,
Joos Vanderwalle		 10
SUGI 1994 SAS/GEO-New Tools in the SAS System for Geoscience Professionals Gary S. Franklin,
Delpfine E. Welch		 source 3
WUSS 1993 Is the SAS System a Database Management System? William D. Clifford source 6
SCSUG 1993 Is the SAS System a Database Management System? William D. Clifford 6
SUGI 1993 A GIS Is Born! Francois Tessier,
Michael Beaudry,
Richard Toussaint		 source 5
SUGI 1993 Is the SAS System a Database Management System? William D. Clifford source 6
NESUG 1992 SAS System Supervison - A Version 6 Update Merry G. Rabb,
Donald J. Henderson,
Jeffrey Polzin		 8
NESUG 1990 The SAS Supervisor - A Version 6 Update Donald J. Henderson,
Merry G. Rabb,
Jeffrey A. Polzin		 11
SUGI 1982 An Integration of System 2000 and Statistical Analysis System (SAS) Roger E. Booker source 7
SUGI 1982 The Role of Database Management Systems for Investigative Data Gary Anderson source

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