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clinical research

844 papers and 133 presentations; 924 titles.

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Conference × Year × Title × Authors Extras Pages
WUSS 2026 Smarter CRF Reviews: An Open-Source AI Tool for Automated Protocol-to-CRF Gap Analysis in Clinical Trials Raj Sharma source 9
PharmaSUG CN 2026 AI in Regulatory Submissions: Health Authority Expectations and Emerging Opportunities for Data Standards and Submission He Liu source 7
PharmaSUG CN 2026 An Integrated, AI-Augmented R Shiny Platform for Oncology Clinical Trial Decision Intelligence: From CDISC Data to Go/No-Go in One Unified Hub Zhiping Yan source 28
PharmaSUG CN 2026 Validation Strategy for TLF AI-Generated Results Han Wang,
Zongfeng Lei,
Patick Zhang		 source 7
PharmaSUG 2026 AI-First Leadership in Biometrics: Redefining Strategy, Teams and Execution in the Agentic AI Era Kevin Lee source 7
PharmaSUG 2026 An End-to-End R-Based Pharmacokinetics (PK) Workflow for Regulatory Submission: The INAVO120 Study Qi Liu,
Shweta Vadhavkar		 source 5
PharmaSUG 2026 Analysis Concepts role within the CDISC 360i vision Alyssa M. Wittle,
Brian Harris		 source 5
PharmaSUG 2026 Beyond Today-s Evidence: How AI-Enabled RWE Will Transform Development Speed, Study Quality, and Real-World Impact Sherrine Eid source 15
PharmaSUG 2026 Delegation as a Quality Strategy: Building Accountable Biometrics Teams Steven Tan source 5
PharmaSUG 2026 Early Unblinding to Pharmacometrics (PMx) Data: Challenges, Practices, and Benefits Shweta Vadhavkar,
Jing Su		 source 6
PharmaSUG 2026 From Programmer to Influencer: Strategic Leadership for Statistical Programmers in Clinical Development Xiaohan Zou,
Wei Shao,
Yi Yan		 source 9
PharmaSUG 2026 From SAS Servers to AI Agentic SCEs: Integrating Agentic AI into GxP-Compliant Biometrics Workflows Kevin Lee source 5
PharmaSUG 2026 From Statistical Programmer to Analytical Partner: Navigating the Future of Biostatistics Shivani Gupta source 6
PharmaSUG 2026 Implementing AI Agent-Driven Tools to Accelerate Clinical Research Workflows Nathan Lee source 13
PharmaSUG 2026 Navigating Early Career Challenges in PK/ADA Statistical Programming Diyu Yang,
Sandeep Meesala		 source 11
PharmaSUG 2026 Patient-Level, Dose-Stratified Swimmer Plots for Comparative Adverse Event Time-Course Assessment in Clinical Trials Using SAS PROC TEMPLATE Qingwei Hu,
Zhaoyu Xie,
Ji Qi		 source 5
PharmaSUG 2026 PSMATCH: Propensity Score Matching of Clinical Trial Data with External Control Arms Ginger Barlow source 8
PharmaSUG 2026 Python for Survival Analysis: Kaplan-Meier and Reverse KM Plots Made Easy Girish Kankipati,
Bala Rajesh Jakka		 source 20
PharmaSUG 2026 R Package Management in LSAF: Challenges and Solutions Praneeth Adidela,
Sagar Koona		 source 7
PharmaSUG 2026 Structure-Preserving Preprocessing of Clinical Documents for Large Language Model Analysis Zun Wang,
Juntao Yan		 source 12
PharmaSUG 2026 Unleashing Open-Source Potential in SAS: The PharmaForest Ecosystem (proc pharmaforest data=open_source out=... ;) Sharad Chhetri,
Ryo Nakaya		 source 7
PharmaSUG 2026 Women Leadership in AI-Driven Clinical Programming: Navigating Intersectionality and Innovation Lida Gharibvand source 31
PHUSE US 2026 Acquiring a Compound with Multiple Clinical Trials? Let's Get Ready for a Type C Meeting! Key Considerations for Preparing Its Regulatory Submission Mathura P. Ramanathan,
Kajal Tahiliani		 source
presentation source		 12
PHUSE US 2026 Advancing Transparency, Patient-centricity, and Trustworthiness in Pharma: Metrics and Trends from the Good Pharma Scorecard [presentation] Jennifer Miller source 48
PHUSE US 2026 AI as Copilot: Empowering, Not Replacing, Clinical Statistical Programmers Bhavesh Patkar source
presentation source		 5
PHUSE US 2026 Analysis Concepts Definition: Initial Perspectives from the CDISC Working Group Stuart Malcolm source
presentation source		 4
PHUSE US 2026 Around the Data DOSE-y Doe: Using DOSExx Variables within ADaM Datasets Inka Leprince,
Richann J. Watson		 source 10
PHUSE US 2026 Automated Code Generation: Evaluating Deterministic and Probabilistic Approaches Malan Bosman source
presentation source		 6
PHUSE US 2026 Beyond Box-Checking: Five Best Practices for Embedding QC in Modern SCEs Chris McSpiritt source
presentation source		 6
PHUSE US 2026 Breaking into Statistical Programming: How SAS, R, Python, AI and ML Are Shaping Career Paths Kishore Pothuri source
presentation source		 6
PHUSE US 2026 Bridging Analysis and Strategy: The Transformative Role of Statistical Analysts in Drug Development Lingsong Yun source
presentation source		 17
PHUSE US 2026 C&SP 203X Reinventing Clinical & Statistical programming for the AI - era [presentation] Sangeeta Bhattacharya source 19
PHUSE US 2026 CCI Proposals In Clinical Documents - Gap Analyses [presentation] Radu Popescu,
Silvia Garrido-Lestache		 source 14
PHUSE US 2026 CDISC ARS Template Code: Gearing Up with Automation in TFL Programming Malan Bosman,
Anna Yaggi		 source
presentation source		 7
PHUSE US 2026 CDISC Biomedical Concepts for Breast Cancer: A CDISC 360i Perspective Bess LeRoy,
Brian Harris		 source
presentation source		 2
PHUSE US 2026 Complex Trials, Simple Disclosures: Streamlined Transparency of Innovative Study Designs [presentation] Ritama Gupta Dempsey source 15
PHUSE US 2026 Data Can't Do It Alone: The Untold Power of Soft Skills in IDMCs Maira Pinto source
presentation source		 9
PHUSE US 2026 Data Storytelling: A Crucial Leadership Skill in Today's Clinical Research Landscape Bhavesh Patkar source
presentation source		 9
PHUSE US 2026 Democratising SDTM Transformations: AI-Assisted Function Development with Business-Driven Governance Ulf Nielsen,
Rostislav Markov		 source
presentation source		 11
PHUSE US 2026 Deterministic Foundations, AI Acceleration: Lessons from Developing Hybrid Clinical Review Tools Matthew Kumar,
Srinivas Veeragoni		 source
presentation source		 8
PHUSE US 2026 Electronic Submission of Population PK Analysis Files ... What's Your Modus Operandi? Luai R. Alzoubi source
presentation source		 13
PHUSE US 2026 Empowering Clinical Data Review with Interactive Patient-Level Visualisations in {teal} Dony Unardi source 4
PHUSE US 2026 Enabling Innovation: Lessons from the CDISC AI Innovation Challenge Julie Smiley source
presentation source		 10
PHUSE US 2026 Enhancing Clinical Trial Dataset Mapping with AI/ML Techniques: An Approach for CDISC Variable Prediction Parvee Kumar source
presentation source		 7
PHUSE US 2026 Ensuring Reliability of Medical Devices Through Statistical Oversight in the Age of AI Parvee Kumar,
Shrutimita Pokhariyal		 source
presentation source		 11
PHUSE US 2026 From Automation to Audit-Readiness-AI's Growing Role in Statistical Programming Manoj Kumar Maripally source
presentation source		 4
PHUSE US 2026 From Demo to Deployment: Bridging the AI Implementation Gap Melanie Hullings,
Emily Yates		 source
presentation source		 5
PHUSE US 2026 From Git Init to GitHub Push: A Complete Version Control Workflow for Statistical Programming Jeetender Chauhan source
poster source		 14
PHUSE US 2026 From System Exports to Standards: Will Standardisation of External Vendor Data Redefine Clinical Data Management/Analysis? Sai Sri Sravya Deevi source
presentation source		 5
PHUSE US 2026 Introduction of PharmaForest - Forest of SAS packages Ryo Nakaya,
Hiroki Yamanobe,
Yutaka Morioka		 source
presentation source		 7
PHUSE US 2026 Leveraging Python for Synthetic External Vendor Data Generation for eCOA and ePRO Hitesh Raval source
presentation source		 9
PHUSE US 2026 Modernising Statistical Computing Environments: Scalable, AI-Ready and GxP-Compliant by Design Amanda Lopuski,
Rafael Pereira		 source
presentation source		 7
PHUSE US 2026 Next Generation QC Workflow Optimisation: Current Practices and Future Directions from the Emerging Trends & Innovation Working Group Matthew Finnemeyer,
Caroline Phares		 source
presentation source		 13
PHUSE US 2026 Open Source Pavilion: Metadata-driven Automation Interactive [presentation] Orla Doyle,
Rammprasad Ganapathy		 source 28
PHUSE US 2026 Optimising Flexibility and Consistency in Statistical Programming for Platform Trials: Practical Approaches to Data Cut, SDTM, ADaM and TFL Setup Kelly Fang,
Zhen (Laura) Li		 source
poster source		 6
PHUSE US 2026 Orchestrating Multi-Agent Workflows for Complex Trial Data Integration Rajesh Hagalwadi source 8
PHUSE US 2026 PHUSE Working Groups Highlights [poster] Chris Price source 1
PHUSE US 2026 Problem-First Agentic AI: Transforming Statistical Computing with Purposeful Automation Rajesh Hagalwadi source
presentation source		 8
PHUSE US 2026 Protecting Commercially Confidential Information (CCI) Under the EU Clinical Trials Regulation [presentation] Christa Polidori,
Sanjay Bagani		 source 4
PHUSE US 2026 Regul-ASIAN Uncovered Navigating Reporting Requirements in Asian Markets [presentation] Ben Evans source 42
PHUSE US 2026 Rethinking Data Quality - From Fragmented Checks to Connected Insights Eva Kelty source
presentation source		 6
PHUSE US 2026 Risk-Driven AI Oversight in Clinical Research: A Tiered Framework Using ISO, ICH Q9 and FMEA Laxmiraju Kandikatla,
Rajesh Hagalwadi		 source
presentation source		 9
PHUSE US 2026 Scaling Biometric Teams in Emerging Regions: Lessons from Armenia Nairi Alikhanyan,
Arman Melkonyan		 source
presentation source		 7
PHUSE US 2026 Scaling for the Future: Transitioning from In-House to Commercial Statistical Computing Environments Hemu Shere,
Majdoub Haloui		 source
presentation source		 8
PHUSE US 2026 SCE White Paper 2.0 - A Modernised Framework for the Next Generation of Data Analysis Mark Bynens source
presentation source		 7
PHUSE US 2026 SpecToSAS: AI-Powered SAS Code Generation from Study Specs Gargee Vaidya,
Lluis Gimenez		 source
presentation 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 Clinical Data Lake: Empowering the Data Caterer Vision with Veeva, SAS and Open Source Sascha Ahrweiler,
Holger Dach		 source
presentation source		 7
PHUSE US 2026 The Curious Case of External Controlled Arms (ECAs): Practical Solutions for External and RWD Integration Manish Deole,
Preethi Samala		 source
presentation source		 6
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 SMART + Framework for AI Systems Laxmiraju Kandikatla source
poster source		 9
PHUSE US 2026 Transforming Clinical Trials: Present Innovations and Future Paths with AI and Agentic Tools Sandeep Purwar source
presentation source		 5
PHUSE US 2026 Trends in eSub Evaluation Findings: A Twenty-Year Perspective on Data Traceability Lisa Kaye Brooks source
presentation source		 9
PHUSE US 2026 Validation Strategies for Agentic AI Platforms in GxP-Regulated Clinical Data Environments Rajesh Hagalwadi source
presentation source		 9
PHUSE US 2026 Voice-Driven Agent-Assisted Open-Source Data Science Philip Bowsher source
presentation source		 10
PHUSE US 2026 Your Brain on AI: What We Gain, What We Risk, and How To Harness AI Without Losing Trial Integrity Aditya Gadiko source
presentation source		 6
PHUSE APAC 2026 Accelerating Pharma Innovation: The Role of SAS Synthetic Data Soundarya Palanisamy,
Anand Phand		 source
presentation source		 7
PHUSE APAC 2026 Accelerating Productivity: Understand How SAS Viya Copilot Helps Users Work More Effectively Across the Analytics Life Cycle Ajay Tomar source
presentation source		 6
PHUSE APAC 2026 Advancing Clinical Programming Through Centres of Excellence Surendra Yajamanam source
presentation source		 3
PHUSE APAC 2026 AI for Adverse Event Signal Detection: Moving Beyond Monika Monika source
presentation source		 10
PHUSE APAC 2026 AI-Driven Protocol Review: Accelerating and Simplifying Review Aditya Moogi source
poster source		 14
PHUSE APAC 2026 Beyond Code: Elevating NextGen Statistical Programmers through Cross-Functional Learnings Saumil Tripathi source
presentation source		 7
PHUSE APAC 2026 Beyond Toxicity : Accelerating Dose -Finding with Pharmacokinetic -Driven Bayesian Design PKBOIN-12 Anetta Mary Xavier source
presentation source		 13
PHUSE APAC 2026 Bridging Statistical Expertise Through Intuitive Design: A Modern Web Interface for Automated SAS Procedure Selection in Cardiovascular Clinical Trials Likith Gopikumar source
presentation source		 10
PHUSE APAC 2026 CDISC 360i In Action – Demonstrating the Shift to Fully Digital Standards [presentation] Darren Moreland,
Julie Smiley,
Bhavin Busa,
Peter Van Reusel		 source 11
PHUSE APAC 2026 Crafting a recipe for success : Aligning Target Product Profiles and study design to ensure statistical significance translates to clinical relevance and role of DGF Soumitra Kar,
Novo Nordisk GBS		 source
presentation source		 9
PHUSE APAC 2026 Critical & Sensitive Information (CSI) Paper AS02 Revolutionizing Clinical Quality: A Frontier Approach with Quality by Design (QbD), Infrastructure Modernization and Data-Driven Analytics Priti Gupta,
Deepa Balaji		 source
presentation source		 12
PHUSE APAC 2026 Cross-Platform Programming for Clinical Development: Practical Use of SAS, R, and Python Sandeep Lakkol,
Vinay S		 source
presentation source		 7
PHUSE APAC 2026 Development of Statistical Scientists for Pharmaceutical Drug Development at India Global Capability Centres Suresh Chenji source
presentation source		 6
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 APAC 2026 Empowering Clinical Research Teams in the Age of AI: Building Resilience and Innovation in APAC Ashwini Mathur source
presentation source		 13
PHUSE APAC 2026 End-to-End Continuous Integration and Deployment Pipeline for Multi Language Analytics Applications: A Clinical Data Management Case Study Avinash Patnaik,
Varun Sethuraman		 source
presentation source		 7
PHUSE APAC 2026 Enhancing Interpretation of Propensity Score Matching through Advanced Data Visualization in Real-World Studies KiranKumar Vyas,
Umayal Annamalai		 source
presentation source		 7
PHUSE APAC 2026 From Information to Insights: Harnessing Centralized Monitoring in RBQM to proactively identify and mitigate risks in Clinical Trials Bismita Borkakoty,
Priyangshu Chowdhury		 source
presentation source		 12
PHUSE APAC 2026 From Static to Interactive: A Comparative Evaluation of ggplot2 and Plotly in Clinical Data Visualisation Mugdha Joshi source
presentation source		 8
PHUSE APAC 2026 From Uncertainty to Clarity: A Personal Journey in Pharma Data Science Using the Johari Window Ratna Kumari Koganti,
Ramya Pichikala		 source
presentation source		 7
PHUSE APAC 2026 From XPT to JSON for submissions: Are we ready for the change? Poorna Suresh,
Bill Qubeck		 source
presentation source		 20
PHUSE APAC 2026 Future-Focused Real-World Data Use Strategies: Resilience and Innovation at Chugai Wataru Ohtsuka,
Nauta Yamanaka		 source
presentation source		 8
PHUSE APAC 2026 Harnessing Real-World Evidence and Data Visualisation to Improve Clinical Development and Accelerate Patient-Centric, Insight-Driven Decision-Making [presentation] Mujeebuddin Shaik source 20
PHUSE APAC 2026 Integrating R Programming and Generative AI for Prompt-Driven Clinical Trial Data Analysis Vyom Bhatt source
presentation source		 4
PHUSE APAC 2026 Integrating Real-World Evidence (RWE) and Digital Health Technologies (DHTs) with AI for Enhanced Patient Outcomes (RE) Varun Sethuraman source
presentation source		 10
PHUSE APAC 2026 Legacy to Leading Edge: Reinventing Biostats Programming with Technology, AI, and Agile Innovation Deepthi BM source
presentation source		 8
PHUSE APAC 2026 Leveraging Real-World Evidence (RWE) in Clinical Trial Design: Statistical Challenges and Opportunities Muhammed Farzan K source
presentation source		 6
PHUSE APAC 2026 Next-Gen Transport Standards: Dataset-JSON from a Programmer's Lens Venkata Koteswara Rao Rayala source
presentation source		 6
PHUSE APAC 2026 Optimising Few-Shot Prompting Strategies for Scalable and Reliable Enterprise AI Applications Varun Sethuraman,
Avinash Patnaik		 source
presentation source		 10
PHUSE APAC 2026 RbQM: An Intersection of Cross-Functional Collaboration of Clinical, Analytics, Statistics and Technology Domains for Better Clinical Trial Governance Abhishek Ghosh source
presentation source		 10
PHUSE APAC 2026 SAS to R: CHEAT SHEET - A Practical Guide for Clinical Programmers Lekitha JK,
Jalendhar Ettedi		 source
poster source		 24
PHUSE APAC 2026 Signal First: A Data-Driven Approach to Safety Prioritization Using SAS and Tableau Jinu J. Nair,
Rubina Pathan		 source
poster source		 9
PHUSE APAC 2026 Streamlining SEND Dataset Generation: Enhancing Efficiency and Quality with Shiny Dashboards Madhulika Mishra,
Michael Denieu		 source
presentation source		 10
PHUSE APAC 2026 Summary Outputs Made Simple: A Mirror View for SAS Programmers Exploring R Venkata Koteswara Rao Rayala source
poster source		 7
PHUSE APAC 2026 Targeted Maximum Likelihood Estimation: A Unified Approach for Confounding and Selection Bias Mahjoob O. Majeed,
Noel S. John		 source
presentation source		 6
PHUSE APAC 2026 The AI-Powered Scribe: An Agentic Framework for Automated CSR Authoring Allwyn Dsouza source
presentation source		 7
PHUSE APAC 2026 The Expanding Role of Real-World Evidence (RWE) in Supporting Regulatory Submissions Setu Sagar,
Nikhil A		 source
presentation source		 6
PHUSE APAC 2026 The Half-Life of Skills: Leading When Today's Expertise is Tomorrow's Obsolete Pratibha Jalui source
presentation source		 4
PHUSE APAC 2026 Thriving in a Dynamic World: Unlock the Magic of a Growth Mindset Abhishek Mishra source
presentation source		 3
PHUSE APAC 2026 TLF Treasure Hunt: Making Legacy Data Instantly Discoverable with RAD Finder Alexis Bernard Dalam,
Cielo Marie Castañeda		 source
presentation source		 6
PHUSE APAC 2026 Unlock Deeper Clinical Insights: A Unified Approach to Data Analysis with SAS, R, and Python Pavan Kallurkar source
presentation source		 7
PHUSE APAC 2026 Unlocking Biopharma Insights: A RAG-Enabled AI Framework for Rapid Access to Clinical and Nonclinical Study Data Lakshmi B K,
Sapna Chandran		 source
presentation source		 9
PHUSE APAC 2026 Workforce 360°: Future-Proofing Leadership Models Sugumaran Muthuraj source
presentation source		 10
PHUSE EU 2025 Are Study Deliverables Under Your RADAR? Deepak Pandarivasagan,
Piotr Karasiewicz		 source
poster source		 5
PHUSE EU 2025 Aspirations of language agnosticism - experiences expanding the programming stack with python Kaj Arai Hejlesen,
Michael Svingel		 source
presentation source		 9
PHUSE EU 2025 Beyond Authority: Navigating Challenges, Earning Trust and Building High-Performance Teams in FSP and Outsourced Delivery Models Emmanuelle Hoarau,
Tim Southwick		 source
presentation source		 4
PHUSE EU 2025 Beyond the Code: Evolving from Clinical Programmer to Strategic Partner in Clinical Trials Anastasiia Khoba source
presentation source		 4
PHUSE EU 2025 Blockr: Advancing Data Pipelines with DAG-Based Workflows and LLM Orchestration Karma Tarap,
Nicolas Bennet		 source
presentation source		 7
PHUSE EU 2025 Bridging Languages: Building Integrated Analytical Tools with SAS, R, and Python for Clinical Data Margarethe Povey source
presentation source		 7
PHUSE EU 2025 Busy ? Productive: Breaking the Myth of Multitasking Goele Aerts source
presentation source		 8
PHUSE EU 2025 CDISCDataset.com: An AI-Powered Platform for Generating Synthetic CDISC-Compliant SDTM and ADaM Datasets, CRFs, Protocols, TFL Shells, and Specs Ara Baghumyan source
presentation source		 2
PHUSE EU 2025 Clinical Trials in the Quantum Era Michael Cooper,
Edyta Winciorek		 source
poster source		 11
PHUSE EU 2025 Code, Collaborate, Conquer: The Future-Proof Programmer in an AI World James Shipley-Burgess source
presentation source		 4
PHUSE EU 2025 Diversity, Inclusion and Equality Its Just Good Science! Roxanne McGuire,
Chris Ward		 source
presentation source		 19
PHUSE EU 2025 Evaluating the Use of Real-World Data (RWD) as a Synthetic Control Group: A Statistical Approach Vasiliki Economou,
Dimitrios Kounelis		 source
poster source		 17
PHUSE EU 2025 FHIR for RWD Submissions: Why a US Regulation Signals a Global Shift And What You Need To Do Now Sanyogeeta Andhale,
Nachiket Thakkar		 source
presentation source		 11
PHUSE EU 2025 Fit-For-Purpose Approach of RBQM in Small Clinical Trials [presentation] Alicja Mark,
Agnes Verhoeven		 source 15
PHUSE EU 2025 Framework for Integrating Omics Data with Other Clinical and NonClinical Data Sources Mehdi Harek,
Jonathon Keeney		 source
presentation source		 12
PHUSE EU 2025 Human in or Human out of the Loop: Impact and Things To Consider While Deploying AI Olivier Bouchard source
presentation source		 8
PHUSE EU 2025 Human in the Middle: Accelerating with AI, Anchored in Quality Melanie Hullings,
Christopher H. White		 source
presentation source		 6
PHUSE EU 2025 JSON for Submissions: Why You Should Care, What You Need To Know, and What To Do Now Bill Qubeck,
Sridhar Vijendra		 source
presentation source		 13
PHUSE EU 2025 Leveraging Open-Source Python Tools to Improve Efficiency and Transparency in Clinical Trials Sohan Lal,
Michael Olds		 source
presentation source		 8
PHUSE EU 2025 No Patients? No Problem Define Your Study Data with Python at the CORE John McDade source
presentation source		 11
PHUSE EU 2025 PHUSE Working Groups Highlights [poster] Chris Price source 1
PHUSE EU 2025 Redefining the role of the Statistical Programmer in an AI-Driven World James Shipley-Burgess source
poster source		 4
PHUSE EU 2025 Rethinking Automation in the AI Era James Zee,
Liz Cole		 source
presentation source		 4
PHUSE EU 2025 Showcasing a Shiny Tool for Evaluating Biomarkers for Derisking Clinical Trials Stefan Thoma source
presentation source		 9
PHUSE EU 2025 Synthetic Data - the Game Changer in Drug Development Soundarya Palanisamy,
Anette Dalsgaard Jakobsen		 source
presentation source		 7
PHUSE EU 2025 Tried and Tested Principles for Building, Managing and Leading High-Performing Teams Through Challenging Initiatives Caroline Phares,
Oliver Robinson		 source
presentation source		 5
PHUSE EU 2025 What We Gained (and Lost) by Using Python in SDTM Conversions [presentation] Katarzyna Bzymek source 25
PHUSE EU 2025 Why Wait for Real Data? The Power of Synthetic Data in Modern Clinical Trials Abhijeet Arora source
presentation source		 6
MWSUG 2025 Automated double data entry comparisons [presentation] Melinda MacDougall source 10
MWSUG 2025 Maps, maps, and more maps using SAS PROC SGMAP! [presentation] Melinda MacDougall source 40
SESUG 2025 Craft Your Career as a Statistical Programmer: Opportunities and Challenges at CROs vs. Pharmas Xiao Xiao 6
SESUG 2025 The Business Value of Diversity Combined with Data Science Stephen B. Sloan 5
WUSS 2025 Around the Data DOSE-y Doe, How Much Fun Can Your Data Can Be: Using DOSExx Variables within ADaM Data Sets Inka Leprince,
Richann J. Watson		 source 13
PharmaSUG 2025 AI is coming for you: New Biometric Leadership in the era of Gen AI Kevin Lee source 7
PharmaSUG 2025 AI-Powered Data Issue Tracker for Efficient Data Issue Tracking and Resolution Bharath Donthi source 6
PharmaSUG 2025 Breaking Barriers in Clinical Trials: Insights into Platform Designs Chetankumar Patel source 11
PharmaSUG 2025 Building a Scalable Training Platform for R: Empowering Analytics Excellence in Corporate Initiatives Michelle Page-Lopez,
Martyn Walker		 source 7
PharmaSUG 2025 Building Resilient Teams Patrick Grimes,
Sajin Johnny		 source 15
PharmaSUG 2025 Deciphering Exposure-Response Analysis Datasets: A Programmer-s Perspective for Oncology Studies Sabarinath Sundaram source 6
PharmaSUG 2025 Elevating Clinical Research: Strategic Implementation of CDASH and SDTM Standards Hayden Patel source 4
PharmaSUG 2025 Embracing Continuous Learning in the Life Sciences Ecosystem Iuliana Constantin source 11
PharmaSUG 2025 Enhancing Dictionary Management and Automation with NCI EVS: A Deeper Dive for the CDISC Community Anthony Chow source 6
PharmaSUG 2025 Ensuring Data Integrity: Techniques for Validating SDTM Datasets in Clinical Research Amy Welsh source 8
PharmaSUG 2025 Follow the Yellow Brick Road: Finding the Critical Path for a Study-s Lifespan Jake Gallagher source 4
PharmaSUG 2025 Generative AI in Biometrics: Transforming Clinical Trials with Supercharged Efficiency an Innovation Kevin Lee source 6
PharmaSUG 2025 Improve Your CRF Review Process: A Python-Based Approach to Capturing CRFs via Browser Automation Andrew Herndon source 8
PharmaSUG 2025 Integrating Generative AI into Medical Writing: Building an Interactive Drafting and Search Framework Tadashi Matsuno source 12
PharmaSUG 2025 Leading Through Change: Motivating Programming Teams During Mergers and Integrations Shefalica Chand source 11
PharmaSUG 2025 Optimized Resourcing Strategies in Statistical Programming within CROs and Considerations for AI Integration in Resource Management Vihar Patel source 10
PharmaSUG 2025 Promising Zone Designs for Sample Size Re-estimation in Clinical Trials: Graphical Approaches Using SAS Zhao Yang,
Shivani Nanda		 source 18
PharmaSUG 2025 R Programming in SAS LSAF: How to Generate Clinical Reports Using an R Session Praneeth Adidela source 12
PharmaSUG 2025 Streamlining and Accelerating Clinical Research through AI and GenAI driven Insights and safety review of Medical and Scientific Literature Rohit Kadam,
Saurabh Das,
Rajasekhar Gadde,
Niketan Panchal,
Alejandra Guerchicoff		 source 6
PharmaSUG 2025 Understanding HIV: At-Risk Populations, Treatment, Prevention and Standardized Data Representation in HIV Studies Jyoti (Jo) Agarwal source 12
PharmaSUG 2025 Unlocking Insights: Comparative Analysis of CRF Changes with R Shiny Mayank Singh source 5
PharmaSUG 2025 Zero to Hero: The Making of a Comprehensive R Shiny Figures App Yi Guo,
Matthew Salzano,
Nicholas Sun,
Sean Healey		 source 30
PHUSE US 2025 A Customized Algorithm to Evaluate the Quality and Reliability of Real-World Lab Data Lihai Song source
presentation source		 10
PHUSE US 2025 A Guided User Experience for Automated Mapping Nathan Johnson source
presentation source		 9
PHUSE US 2025 Adapting Leadership in Statistical Programming: Navigating Technological Advancements and Evolving Roles in the Pharmaceutical Industry Jaya Mukkamala source
presentation source		 2
PHUSE US 2025 AI Ethical Considerations in Drug Development and Regulatory Review Tara Chavda,
Qingying Ally Lu		 source
presentation source		 5
PHUSE US 2025 Big Data Analytics: Unlocking Insights from Vast Clinical Datasets Bill Qubeck,
Kala Shivalingaiah		 source
presentation source		 16
PHUSE US 2025 Biomedical Concepts: What Are They and Why Should I Care? Stuart Malcolm source
presentation source		 7
PHUSE US 2025 Building Rome in a Few Months: How Open-Source Technologies Empower Small Pharma Chendi Liao,
Kasra Yousefi		 source
presentation source		 5
PHUSE US 2025 Can AI Help Overcome the Validation Burden for Open Source? Marc Jantke source
presentation source		 8
PHUSE US 2025 CDISC 360i: Implementing the CDISC Roadmap Connecting Standards from Design to Analysis Chris Decker,
Peter Van Reusel		 source
presentation source		 4
PHUSE US 2025 CDISC Open Rules: A Deep Dive into Custom Rule Creation Roman Radelicki source
presentation source		 12
PHUSE US 2025 Challenges of Genomic Data in Clinical Trials Hong Zheng,
Lingsong Yun		 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 Digital Health Technologies: Evolution, Insights and Future Directions [presentation] Vijay Pasapula source 28
PHUSE US 2025 Dismantling the Black Box: Why We Need to Think Bigger About AI Integration Christina Dinger,
Joe Lebers		 source
presentation source		 7
PHUSE US 2025 Dynamic Survival Model for Monitoring Resistance Mutations in Targeted Therapy: Advancing Precision Medicine in Oncology Hong Zheng source
presentation source		 5
PHUSE US 2025 Effective Adverse Event Management Eva Kelty,
Catharina Dahlbo		 source
poster 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 Enhancing the (ASAP) Aggregate Safety Assessment Planning Framework with an Interactive R Markdown Application: Seeing is believing! Debopriya Ghosh source
presentation source		 7
PHUSE US 2025 eProtocol and the Promise of Automation Bill Qubeck,
Suhas Giriraj		 source
presentation source		 17
PHUSE US 2025 From Application to Approval: Exploring the FDA's Review Process Kiran Bonda source
presentation source		 4
PHUSE US 2025 From Data Manager to Data Scientist: Navigating the Future of Data Management in Clinical Trials Debra Anderson source
presentation source		 6
PHUSE US 2025 From Fragmentation to Fusion: A Journey through Mergers and Acquisitions Data Integration Challenges Xiao Huang source
presentation source		 3
PHUSE US 2025 From Manual to Machine: Leveraging Best-of-Breed Approaches in Clinical Data Management Joseph Lebers source
presentation source		 10
PHUSE US 2025 From Topline to Triumph: Visualising the Pathways to Regulatory Approval Jasperlynn Kao source
poster source		 5
PHUSE US 2025 Future-Proofing Clinical Data Standards: Preparing for AI and Machine Learning Shivoy Pandita source
presentation source		 8
PHUSE US 2025 Gen AI-Powered Trial Performance Co-Pilot to Accelerate Clinical Trials Venkata Sureshbabu Bondu,
Mohit Sehgal		 source
presentation source		 4
PHUSE US 2025 GPT-Powered Data Insights: Advancing Clinical Data Analytics with Large Language Models (LLMs) Melanie Hullings source
presentation source		 5
PHUSE US 2025 Harmonising Heterogeneity: Orchestrating Innovation Through Interdisciplinary Collaboration and Strategic Alignment Dorothy Dlamini,
Srinivas Veeragoni		 source
presentation source		 5
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 Health Authority Interactions and Communication During the Submission Process Ritesh Dhimmar,
Raman Bassi		 source
presentation source		 5
PHUSE US 2025 How Unique is it for the Subject Identifier in a Study To Have Multiple Screenings and Enrolments? Anahita Vyas,
Rama Kudaravalli		 source
presentation source		 8
PHUSE US 2025 Interactive Dashboards - Empowering Clinicians to Generate Reports Instantly Inderjeet Arora source
presentation source		 8
PHUSE US 2025 Kraken: A Shiny Application for Visualising SDTM Data in Early-Phase Clinical Trials Rutu Patel source
presentation source		 12
PHUSE US 2025 Leadership Presentations: Adapting to the Future: How CROs are Evolving to Meet the Shifting Landscape of Programming and Analysis Generation [presentation] Lavanya Peddibhotla source 10
PHUSE US 2025 Leadership Presentations: How and Why, Statistical Programming Leaders Need to Plan for Next Generation Statistical Programming [presentation] Francis Kendall source 29
PHUSE US 2025 Leadership Presentations: Turning Disruption into Opportunity - Guiding Teams Through AI-Powered Transformation [presentation] Li Zheng source 20
PHUSE US 2025 LLMs in Clinical Trials: Overcoming Challenges Related to Patient Confidentiality and Intellectual Property Amit Javkhedkar,
Samip Shah		 source
presentation source		 7
PHUSE US 2025 LLMs in Drug Development - The Future is Closer Than We Think Chris McSpiritt source
presentation source		 9
PHUSE US 2025 Optimising AI Software for Automated Protection of Personal and Commercially Sensitive Data Honz Slipka source
poster source		 7
PHUSE US 2025 Optimizing Development and Regulatory Submission of eSUB Package for Exposure-Response and PK/PD Analysis Saumilkumar Tripathi,
Ephicacy Lifescience		 source
presentation source		 10
PHUSE US 2025 Posit Team: Metadata-Driven Risk Assessment and Surfacing Validated R Packages Philip Bowsher,
Michael Mayer		 source
presentation source		 5
PHUSE US 2025 Python's Future in Clinical Trials: Innovations and Collaborative Advancements Shweta Shukla,
Sohan Lal		 source
presentation source		 10
PHUSE US 2025 Real-World Data - Analysis-Ready Datasets: A Standardised, Specialised and Innovative Data Solution for Efficient Real-World Data Analysis Nayan Chaudhary,
Navdeep Pal		 source
presentation source		 12
PHUSE US 2025 Revolutionising Clinical Trials: Gen AI-Powered Biometrics Breakthroughs Kevin Lee source
presentation source		 6
PHUSE US 2025 Risk Based Quality Management (RBQM) in Clinical Data Management Marcin Kot,
Anna Górecka		 source
presentation source		 9
PHUSE US 2025 Risk-Informed Data Strategies to Streamline Trial Complexity Tiina Erb source
presentation source		 3
PHUSE US 2025 Role of PK/PD, Biomarker Analysis in the Expansion of Phase 1 Trials Lavanya Peddibhotla source
presentation source		 7
PHUSE US 2025 Streamlining Machine Learning Modelling in Neuroscience Clinical Trials Through Cross-Functional Collaboration Jing Dai source
presentation source		 5
PHUSE US 2025 Surviving a Sunset: Being Resilient in the Face of Open-Source Disruption Franklin E. Menius source
presentation source		 5
PHUSE US 2025 The Best of Both Worlds: Machine Learning and Human-in-the-Loop Processing in TFl Design, Production and Validation Steve Ross,
Ilan Carmeli		 source
presentation source		 6
PHUSE US 2025 The Future of Data Surveillance in Clinical Studies: A Comprehensive Approach to Data Monitoring Using an R Shiny Application for Study Health Jacky Jin,
Ruchitbhai Patel		 source
presentation source		 5
PHUSE US 2025 The Olympics of Data Ingestions Cathryn Herbst source
presentation source		 8
PHUSE US 2025 Transforming Clinical Trials with AI-Driven Protocol Optimization and Next-Gen Statistical Programming Ravindra Shukla source
presentation source		 8
PHUSE US 2025 Transforming Clinical Trials: Leveraging Bayesian Statistics in Innovative Trial Design, Analysis, Applications and Navigating Challenges Jaskaran Singh Saini source
presentation source		 11
PHUSE US 2025 Unlocking the Secrets of Health: A Unified Approach to Biomarker and Clinical Data Integration Pavan Kumar Tatikonda source
presentation source		 8
PHUSE US 2025 Verify: A First-in-Class Review and Validation Platform for Biometrics in Clinical Research Achinoam Ravet Perel source
presentation source		 3
PHUSE US 2025 Wearable Technology: Enhancing Patient Monitoring and Real-World Evidence Bill Qubeck,
Sridhar Vijendra		 source
presentation source		 15
PHUSE US 2025 Your SCE is Only as Good as Your Data: The Central Role of Information Governance in Clinical Research Michelle Chen source
presentation source		 3
PHUSE EU 2024 A Guided User Experience for Automated Mapping Achilleas Zaras source
presentation source		 9
PHUSE EU 2024 Agile Leadership: Inspiring Resilience, Open Collaboration, and Creative Problem-Solving for Outcome-Based Continuous Innovation Bhavesh Patkar source
presentation source		 6
PHUSE EU 2024 Artificial Intelligence Potential Use Cases in Clinical Data Engineering Deepak Pakalapati,
Mounika Pillamarapu		 source
presentation source		 8
PHUSE EU 2024 Behind the Blind: Enhancing Clinical Data Management with Python Niels Schrauwen source
presentation source		 5
PHUSE EU 2024 Block by Block: introducing blockr, the Flexible Open-Source Dashboard Builder Karma Tarap,
Jean-Philippe Coene		 source
presentation source		 7
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 DaVinci: A Modular Framework for Interactive Data Exploration and Visualisation in Clinical Research Isabel Glauß,
Stefan Döring		 source
presentation source		 5
PHUSE EU 2024 Debugging Leadership: Cracking the Code of Statistical Programming Teams in Pharma Jessica Hirsch,
Vitali Gering		 source
presentation source		 2
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 End-to-end Automation Using a Model-Driven Development (MDD) Workbench Stuart Malcolm source
presentation source		 7
PHUSE EU 2024 Failed Clinical Trials: How to Benefit From Negative Experience Anna Amosova source
presentation source		 13
PHUSE EU 2024 From Senior Programmer to Head-of-Function: taking that 'leap-of faith' Roxanne McGuire source
presentation source		 5
PHUSE EU 2024 Introduction to the ADNCA ADaM Charlotte Hampson,
Florence Horspole		 source
poster source		 4
PHUSE EU 2024 Leveraging Data Science and Analytics to Optimise Clinical Trial Execution Melanie Hullings source
presentation source		 4
PHUSE EU 2024 Leveraging Shiny Modules for Modular and Scalable Web Applications for Clinical Trials/Research Sohan Lal,
Pinku Hooda		 source
presentation source		 10
PHUSE EU 2024 Leveraging the USDM Standard in OpenStudyBuilder for Enhanced Data Exchange Marius Conjeaud source
presentation source		 7
PHUSE EU 2024 Navigating the Clinical Research Landscape: The Role of Regulatory Intelligence and LLMs Federica Citterio,
Soundarya Palanisamy		 source
presentation source		 9
PHUSE EU 2024 R Scripts for Streamlining Non-Compartmental Analysis (NCA): A Data Programmer's Dream Valentin Legras source
presentation source		 2
PHUSE EU 2024 Revolutionising Statistical Programming Activities - StatProg CoPilot Consortium Leveraging on Open-Source World and Generative AI Sébastien Tourlet source
presentation source		 4
PHUSE EU 2024 Standards Implementation with a Knowledge-Driven, AI-Powered Platform Roger Gagali Angoh source
presentation source		 3
PHUSE EU 2024 Stop Chatting, Start Scanning: AI's Visual Takeover in Pharma for Data Extraction with the Power of LLMs Ercan Suekuer source
presentation source		 3
PHUSE EU 2024 The Prentice-Wilcoxon Test to Study Time to Healing for Split Face, Double Blind, Dermatology Clinical Trials Shrutimita Pokhariyal,
Craig Wesselman		 source
presentation source		 10
PHUSE EU 2024 Trustworthy and responsible AI in health care and life sciences from a leadership perspective Mark Lambrecht source
presentation source		 3
PHUSE EU 2024 Unlocking the Enigma: Exploring SAS and R Strategies for Handling Non-Printable and Special Characters Eldho Alias,
Vishal V Nair,
Pooja Pradeep Pillai		 source
presentation source		 11
PHUSE EU 2024 Working with Omics data - A Statistical Programmers perspective Adrian Czaban source
presentation source		 10
PHUSE EU 2024 {SAS to R-evolution}: A Statistical Programming Team Journey [poster] Charlotte Cheinin source 1
SESUG 2024 A SAS MACRO to parse clinical conductor timesheets Kennedy Kamau Gachigi source 6
SESUG 2024 The Essentials Given - Becoming an Expert of Statistical Programming in Pharma & Health Care Industry Hongbo Li source 5
WUSS 2024 The Business Value of Diversity Combined with Data Science Stephen B. Sloan source 5
WUSS 2024 Training Domain Specific AI for Clinical Data: Developing an AI Agent to Transform EDC Data to CDISC SDTM and then to ADaM Standards Sy J. Truong source 12
PharmaSUG CN 2024 An Efficient R Shiny App for Exposure-Response Relationship (E-R) Analysis in Oncology Drug Development Zhenghao Chu source 28
PharmaSUG CN 2024 Biomarker Analysis Data Centralization Platform: Accelerators for data analysis automation Jinzhi Zhou,
Jiazheng Zhang,
Linxin Zhang,
Jie Liu		 source 5
PharmaSUG CN 2024 Deep Dive into IB and DSUR: A Compound Lead Programmer's Perspective Yang Song source 7
PharmaSUG CN 2024 Implementation on concentration-QTc modeling Daoqing Li,
Deli Cao		 source 20
PharmaSUG CN 2024 One-stop solution for QA - Automation Tool by Python Yangxue Ma source 5
PharmaSUG 2024 A Change is Gonna Come: Maintaining Company Culture, Managing Time Zones, and Integrating Teams after a Global Acquisition Lydia King source 3
PharmaSUG 2024 A New Way to Automate Data Validation with Pinnacle 21 Enterprise CLI in LSAF Crystal Cheng source 7
PharmaSUG 2024 A Programmer-s Insight into an Alternative to TQT Study Data Submission Hiba Najeeb,
Raghavender Ranga		 source 7
PharmaSUG 2024 Advancing the Maturation of Standardized CRF Design Sugumaran Muthuraj,
Rubha Raghu		 source 9
PharmaSUG 2024 AI and the Clinical Trial Validation Process - Paving a Rocky Road Steve Ross,
Ilan Carmeli		 source 7
PharmaSUG 2024 Around the Data DOSE-y Doe, How Much Fun Can Your Data Can Be: Using DOSExx Variables within ADaM Data Sets Inka Leprince,
Richann J. Watson		 source 12
PharmaSUG 2024 Bayesian Methods in Survival Analysis: Enhancing Insights in Clinical Research Vadym Kalinichenko source 11
PharmaSUG 2024 Bridging AI and Clinical Research: A New Era of Data Management with ChatGPT Illia Skliar source 12
PharmaSUG 2024 Embracing Diversity in Statistical Computing Environments: A Multi-Language Approach Amit Javkhedkar,
Sridhar Vijendra		 source 6
PharmaSUG 2024 Facilitating Seamless SAS-to-R Transition in Clinical Data Analysis: A Finetuned LLM Approach Chaitanya Pradeep Repaka,
Santhosh Karra		 source 6
PharmaSUG 2024 Game changer! The new CDISC ADaM domain ADNCA for PK/PD data analysis Santosh Ranjan source 7
PharmaSUG 2024 I Want to Break Free: CRF Standardization Unleashing Automation Laura Fazio,
Andrew Burd,
Emily Murphy,
Melanie Hullings		 source 6
PharmaSUG 2024 Leadership Lessons from Another Life: How my Previous Career Helped Me as a Statistician Christiana Hawn,
Lily Ray		 source 5
PharmaSUG 2024 Methodology for Automating TOC Extraction from Word Documents to Excel Jeetender Chauhan,
Madhusudhan Ginnaram,
Sarad Nepal,
Jaime Yan		 source 5
PharmaSUG 2024 One size does not fit all: The need and art of customizing SCE and MDR for end users Shilpa Sood,
Sridhar Vijendra		 source 6
PharmaSUG 2024 Ongoing Trends and Strategies to Fine-tune the CRO/Sponsor Partnership - Perspectives from Statistical Programming Mathura P. Ramanathan source 10
PharmaSUG 2024 Optimizing Clinical Data Processes: Harnessing the Power of Metadata Repository (MDR) for Innovative Study Design (ISD) and Integrated Summary of Safety (ISS) / Efficacy (ISE) Lakshmi Mantha,
Purvi Kalra,
Arunateja Gottapu		 source 9
PharmaSUG 2024 Protocol Amendments and EDC Updates: Downstream impact on Clinical Trial Data Anbu Damodaran,
Ram Gudavalli,
Kumar Bhimavarapu		 source 11
PharmaSUG 2024 Submitting Patient-Reported Outcome Data in Cancer Clinical Trials - Guidance for Industry Technical Specifications Document [presentation] Flora Mulkey source 48
PharmaSUG 2024 Utilizing Data Visualization for Continuous Safety and Efficacy Monitoring within Early Development Margaret Wishart,
Tamara Martin		 source 5
PharmaSUG 2024 Visual discovery in Risk-Based Monitoring using topological models Kostiantyn Drach,
Iryna Kotenko		 source 31
PHUSE US 2024 Auditing an Open-Source Software Framework in a Regulatory Environment: Challenges, Gaps and Recommendations Uday Preetham Palukuru,
Shahrzad Talebian		 source
presentation source		 5
PHUSE US 2024 Automation of Exploratory Report Generation using R shiny and R Markdown Denny Sebastian source
poster source		 7
PHUSE US 2024 Bioinformatics Tools in Digital Health and Remote Monitoring Sugumaran Muthuraj,
Barath Baskaran		 source
presentation source		 7
PHUSE US 2024 Case study of verification and validation methods for algorithmic predictive biomarkers Kartik Shetty source
presentation source		 4
PHUSE US 2024 ChatGPT and AI/ML-Empowered Websites for All Jayapandian Nagamalaiyan source 5
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 Embracing the Future of Digitisation: Uninterrupted Data Flows from Protocol Design to Electronic Data Capture [presentation] William Illis,
Diana Ye		 source 18
PHUSE US 2024 Empowering Excellence: Strategies for Cultivating a Culture of Bold Decision-Making in Teams Mark Bynens source 8
PHUSE US 2024 Empowering Healthcare Through Generative AI Ravindra Shukla,
Aman Bahl		 source
presentation source		 7
PHUSE US 2024 Enabling the Breakthroughs of Tomorrow: The Data Lakehouse for Clinical Trials Venu Mallarapu source
presentation source		 12
PHUSE US 2024 Enabling the Interoperable Data Ecosystem with the elluminate Clinical Data Cloud [presentation] Nathan Johnson source 15
PHUSE US 2024 Fidelity Assessment of Real-World Data (RWD) as an External Control Arm Mohamed Sameer,
Umayal Annamalai		 source
poster source		 5
PHUSE US 2024 Front-Loading Statistical Programming Using Automated Synthetic Data Faezeh Moshfeghifar,
Hemanth Padmakar		 source
presentation source		 5
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 Future-Proofing Clinical Data Sciences: The Pivotal Role of Therapeutic Area Proficiency Sascha Ahrweiler source
presentation source		 12
PHUSE US 2024 Identifying Data Quality Issues in Clinical Trials Using OpenAI Embeddings Yash Shah,
Ashwin Rai		 source
presentation source		 5
PHUSE US 2024 Leading Teams Through Clinical Data Transformation with Storytelling Alison Banda,
Katrina Rice		 source
presentation source		 3
PHUSE US 2024 Mining Historical Data and Epidemiological Evidence for Real-World Studies Shubhranshu Dutta source
poster source		 13
PHUSE US 2024 Navigating RBQM Change Management: Real-World Strategies for Success Jamie O'Neill source
presentation source		 4
PHUSE US 2024 Navigating the Safe Integration of AI (ChatGPT) into Clinical Trials Programming Workflow Mykyta Vysotskyi source
presentation source		 10
PHUSE US 2024 Optimizing Clinical Research: Using AI for Automated Validation of Output Tables against ADaM Steve Ross source
presentation source		 5
PHUSE US 2024 Post-Pandemic Trends in Study Designs Charumathy Sreeraman,
Jisha George		 source
presentation source		 7
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 Software Product Lines Framework: How to Manage End-to-End Metadata-Driven Automation at Sale Stuart Malcolm source
poster source		 5
PHUSE US 2024 Spline Analysis to Understand the Non-linear Relationship in Clinical Research Anwaya Joshi source
presentation source		 9
PHUSE US 2024 The Implementation of Scrum in Pharmaceutical Data Analytics and Statistical Programming at Jazz Pharmaceuticals Eliana D'Angelo source
presentation source		 6
PHUSE US 2024 The Potential Power of Data Eva Kelty,
Catharina Dahlbo		 source
presentation source		 5
PHUSE US 2024 Unveiling the Potential of ADNCA via the CDISC ADaM IG: Revolutionising Pharmacokinetic Non-Compartmental Analysis Input Data Standardisation Saumilkumar Tripathi source
presentation source		 10
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 A Beginner's Guide to Overcome the Attrition Bias in Clinical Research: The Method of Inverse Probability of Attrition Weighting (IPAW) Parichay Srivastava source
presentation source		 9
PHUSE EU 2023 Automation and Orchestration of Data Science Applications Using OpenAPI Dmitry Zakharov,
Alexander Lüders		 source
presentation source		 3
PHUSE EU 2023 Avoid Major Pitfalls When Using Real-World Evidence (RWE) in Regulatory Submissions Alex Ide,
Mark Lambrecht		 source
presentation source		 3
PHUSE EU 2023 Be Future-Minded While Designing Your Next Generation SCE Susanne M. Andersen,
Olivier Bouchard		 source
presentation source		 12
PHUSE EU 2023 Becoming an Integrated Part of the Open-Source Pharma Community Philip Bowsher source
presentation source		 11
PHUSE EU 2023 Boosting SAS Programming Efficiency with ChatGPT: A Clinical Trials Perspective Illia Skliar source
presentation source		 11
PHUSE EU 2023 Developing and Implementing CDISC CORE rules: from zero to hero Marisa Wyckmans source
presentation source		 8
PHUSE EU 2023 Driving Better Health for More People - SAS Life Science Analytics William Kuan,
Olivier Bouchard		 source
presentation source		 8
PHUSE EU 2023 Empowering Paediatric Drug Development: CDISC Standards and ICH Guidelines for Clinical Trials with Little Participants Ninan Luke source
presentation source		 5
PHUSE EU 2023 GPT (Generative Pretrained Transformers) and LLM (Large Language Models) have generated a lot of attention since their inception in early 2023 with the advent of OpenAI GPT3.5, then GPT4.0 Jerome Vetillard,
Mark Lambrecht		 source
presentation source		 16
PHUSE EU 2023 Heading to Base Camp On Our Way Up the Open-Source Mountain... Andy Nicholls source
presentation source		 4
PHUSE EU 2023 Human BioGeography: predicting clinical trials outcome using a 3D human body simulation with a GIS framework Diego Caso,
Rocio Matesanz Sanchez,
PhD Student		 source
presentation source		 6
PHUSE EU 2023 Increasing Trend of Biomarker Analysis in Clinical Trials Anjali Ranga source
presentation source		 11
PHUSE EU 2023 Integrating Isolated Clinical Trial Systems with RESTful APIs: Enhancing Data Accessibility and Collaboration Sumesh Kalappurakal,
Nicolas Dupuis		 source
presentation source		 7
PHUSE EU 2023 Optimizing Clinical Trial Design with Real-Time Sample Size Calculation and Enrollment Projection: A Shiny Dashboard Solution Dony Sabu source
presentation source		 5
PHUSE EU 2023 Patient Profiles v2.0: Easy and Quick Clinical Trial Insights in Tableau Roman Radelicki,
Annelies Van Zeveren		 source
presentation source		 6
PHUSE EU 2023 Red Pill or Blue Pill? Assessing the Impact of Artificial Intelligence on Pharmaceutical Programming Paul Shannon source
presentation source		 6
PHUSE EU 2023 SAS Packages for Clinical Programming Eldho Alias,
Prasanth Prabhakaran,
Rahulraj V R		 source
presentation source		 7
PHUSE EU 2023 Statistical Programming 101 for the Fourth Industrial Revolution Ritika Aggarwal source
presentation source		 10
PHUSE EU 2023 Stay Ahead of the Curve: Learn About Leapfrogging as a Statistical Programmer Jitendra Singh,
Kavita Dargan		 source
presentation source		 4
PHUSE EU 2023 Streamlining Clinical Data Analysis and Reporting with R: Best Practices, Tips and Techniques for Efficient Workflow Management and Code Optimisation Vaibhavi Govind Bhide,
Perry Meeks		 source
presentation source		 12
PHUSE EU 2023 Submission Standards for Real-World Data: Gaps, Limitations and Recommendations Jeffrey M. Abolafia,
Sarah Ferko,
Ingeborg Holt		 source
presentation source		 8
PHUSE EU 2023 TFL Automation the CDISC 360 Way Alison Macnab,
John McDade		 source
presentation source		 12
PHUSE EU 2023 The Evolving Role of Statistical Programmers in the Pharmaceutical Industry: The Impact of Artificial Intelligence Cindy Marabotti source
poster source		 8
PHUSE EU 2023 Unleashing the Power of Large Language Models for Clinical Data Approaches: Will AI chatbots like ChatGPT/Bard replace statistical programmer and statisticians over time? Ercan Suekuer source
presentation source		 9
WUSS 2023 Navigating SAS and CDISC Certification with Apprenticeship Sarvar Khamidov source 7
PharmaSUG 2023 A utility to combine study outputs into all-in-one PDF for DSUR Wei Shao source 8
PharmaSUG 2023 An End-to-End and Fully Integrated Clinical Development Platform with eDC/Labs data Data Management, Medical Review, Statistical Analysis and Adaptive Design etc. Peter Wang,
Vindyala Sunil		 source 6
PharmaSUG 2023 Digital Data Flow (DDF) and Technological Solution Providers Prasoon Sangwan,
Piyush K. Singh		 source 8
PharmaSUG 2023 Handling Anti-Drug Antibody (ADA) Data for Efficient Analysis Sabarinath Sundaram,
Johnny Maruthavanan		 source 7
PharmaSUG 2023 Metaverse in the Healthcare - More Real than imagined! Aman Bahl source 14
PharmaSUG 2023 Shifting the drug development paradigm with Adaptive Design and master protocol Aman Bahl source 16
PharmaSUG 2023 Traceability: Not just about Data Rohit Nagpal,
Kavitha Mullela		 source 11
PharmaSUG 2023 Using R to Automate Clinical Trial Data Quality Review Melanie Hullings,
Emily Murphy,
Derek Lawrence,
Michelle Cohen,
Andrew Burd		 source 6
PharmaSUG 2023 What-s the F in specialized people? Let-s talk FSP - the models, variations, and what it takes to be successful Kathy Bradrick,
Ershlena McDaniel,
Lisa Stetler		 source 5
PharmaSUG 2023 What-s the story in your subgroup analysis Lucy Dai source 6
PHUSE US 2023 A Pragmatic Approach to Data Cleaning - Decisions in Selecting When to Apply AI/ML [presentation] Robert Musterer,
Alison Banda		 source 15
PHUSE US 2023 An introduction to NEST, an open-sourced R toolkit for TFL delivery and interactive data displays used in all new Roche trials [presentation] Vincent Shen,
James Black		 source
video		 35
PHUSE US 2023 Build vs Buy for SCE: Considerations for the Future of the Statistical Computing Environment (SCE) [presentation] Nathan Johnson,
Alison Banda		 source
video		 20
PHUSE US 2023 Digging Deep into Digital Biomarkers: Empowering Clinical Trials Vijay Pasapula,
Gianna Huang		 source
presentation source		 12
PHUSE US 2023 Future Workforce: How to invest in your team through Innovative transformation Limna Salim source
presentation source		 8
PHUSE US 2023 If Data is the New Oil, How Do You Make the Most of Your Reserves? Simon Luo,
Ashley Mao		 source
presentation source		 4
PHUSE US 2023 Increasing Use of Chatbots in Mental Health Trials [poster] Vidya Muthukumar source 1
PHUSE US 2023 Making Define-XML Work for You: Considerations in Supporting a Full Schema Implementation [presentation] Carlo Radovsky source 50
PHUSE US 2023 Master Protocol Design: Advantages and Challenges in Vaccine Clinical Trials [presentation] Janaki Shankaran,
Meenal Gawas		 source
video		 19
PHUSE US 2023 SIGMA: What is the Sum of its Impact on Pfizer's Statistical A&R Space? [presentation] Christopher J. Colangelo source
video		 12
PHUSE US 2023 Structured Protocol Authoring (SPA) - A Catalyst for Clinical Protocol Development Suhas Giriraj source
presentation source		 4
PHUSE US 2023 Synthetic Control Arms: Are they the future of Drug Development? [presentation] Sherrine Eid source
video		 16
PHUSE US 2023 The Evolving Role of Project Programmer in The Next 3-5 Years Vinay Gupta,
Manas Rout		 source 5
PHUSE US 2023 Visualised Patient Profiles: Enhanced Timelines for Quick Decision-making [presentation] Jeroen Gielen,
Annelies Van Zeveren		 source
video		 19
PHUSE EU 2022 Agile RnD - From Empiricism to Success Marc Jantke source
presentation source		 8
PHUSE EU 2022 An Approach to Effectively Reproduce TFLs When Performing ADaM Conversion [presentation] Amine Khemiri,
Caroline Pelckmans		 source
video		 19
PHUSE EU 2022 An Automated Approach to Generating Call Programs from an Analysis Request David Maher-McWilliams,
Michael Allie		 source
presentation source		 9
PHUSE EU 2022 Automation of Standard ADaM Variables Through an R Package - GenAdam Mahesh Divakaran source
presentation source		 8
PHUSE EU 2022 Capability Building is the New Normal in the Pharmaceutical Industry Jaganadha Rao Gundu,
Sreekar Mateti		 source 8
PHUSE EU 2022 Collaboration Between Analytical Health Care Technology Leaders will Positively Impact Clinical Trial Research Innovation & Improve Health Care System [presentation] Mark Lambrecht,
Andrew Warrington		 source
video		 19
PHUSE EU 2022 Effective NLP API Access to Unstructured Text for Downstream Analysis and Models in Pharma: Bench to Bedside [presentation] Jane Reed source
video		 26
PHUSE EU 2022 How to Avoid Conformance Issues When Metadata Varies Across Parameters [presentation] Caroline Pelckmans,
Oussama Zineddine		 source
video		 24
PHUSE EU 2022 If You Build it, Will They Come? The Pros and Cons of a Build Versus Buy Strategy for Statistical Computing Environments (SCEs) [presentation] Venu Mallarapu source 13
PHUSE EU 2022 Protocol Deviation Programming [presentation] Oussama Zineddine,
Caroline Pelckmans		 source
video		 25
PHUSE EU 2022 Python to Automate an AR Project Identifying Discrepancies across Fields from a Government Open-source Dataset of COVID-19 Vaccine Registrations Aldir Medeiros Filho source
video
presentation source		 14
PHUSE EU 2022 Scaling within a Fast-moving Biotech Company. Key Learnings for Leaders and Innovators in Our Life Sciences Industry Stijn Rogiers,
Jasmine Kestemont		 source
presentation source		 11
PHUSE EU 2022 Standards Subject to Change: Data Standards Flexibility in an Evolving Landscape [presentation] Gina Wood,
Alison Banda		 source 28
PHUSE EU 2022 The Integration Dilemma Angelo Tinazzi source
video
presentation source		 15
PHUSE EU 2022 Time Goes Fast. Are You Really Ready for Unblinding? [presentation] Stijn Vermeylen source
video		 23
PHUSE EU 2022 Visualise Me! Down the Rabbit Hole with Standardised Dashboards for Safety and Study Follow-up [presentation] Jeroen Gielen,
Stefan Verbeeck		 source
video		 22
PHUSE EU 2022 What's the Difference?! CRO vs Pharma [poster] Tom Ward,
Piotr Karasiewicz		 source 1
PHUSE EU 2022 Who is Subject X? [presentation] Vicky Poulsen,
Henning Pontoppidan Föh		 source
video		 26
WUSS 2022 Complex heatmaps in Statistical analysis of Biomarkers and cancer genomics Yoganand Budumuru source 18
WUSS 2022 Quick Jumpstart into Pharmaceutical SAS Programming Jim Box,
Matthew J. Becker		 source 7
PharmaSUG 2022 A Programmer's Perspective on Patient reported Outcomes in Oncology Trials Divya Vemulapalli source 7
PharmaSUG 2022 Agile innovation - an adaptive approach to transformation in Clinical Research Organizations Aman Bahl,
Hrideep Antony		 source 10
PharmaSUG 2022 Digital Health Technology in Clinical Trials: Opportunities, Challenges and Biometrics Future Re-imagined Kalyan Chakravarthy Buddavarapu,
Sherry Ye,
Vijay Vaidya		 source 12
PharmaSUG 2022 Finding Accord: Developing an eCOA Data Transfer Specification (DTS) All Can Agree On Franklin E. Menius,
Monali Khanna,
Vincent Allibone		 source 12
PharmaSUG 2022 Orchestrating Clinical Sequels with a Strategic Wand - Challenges of introducing Rolling CSRs in a Master Protocol Neharika Sharma source 9
PharmaSUG 2022 Quality Gates: An Overview from Clinical SAS Programming Perspective Nagadip Rao,
Pavan Jupelli		 source 10
PHUSE US 2022 A Better Way: eCOA/ePRO Annotated Screen Reports (aSR) Provide Data Clarity from Data Collection to Submission Franklin E. Menius,
Monali Khanna,
Vincent Allibone		 source
presentation source		 6
PHUSE US 2022 Data Standardization at Scale with the elluminate Clinical Data Cloud [presentation] Nathan Johnson source 19
PHUSE US 2022 Fast and Curious: Reusability with Standardized Dashboards for Safety and Study Follow-up [presentation] Jeroen Gielen,
Roman Radelicki		 source 21
PHUSE US 2022 Finding a New Home-Work Balance: The Importance of Disconnecting Yourself in an Online World [presentation] Annelies Van Zeveren,
Goele Aerts		 source
video		 19
PHUSE US 2022 High-quality COVID Vaccine Submission at Lightning Speed [presentation] Helen Yang,
Kiran Challagali		 source 9
PHUSE US 2022 Leveraging an MDR: More than a Repository [presentation] Carlo Radovsky source 13
PHUSE US 2022 RBM - The New Normal Vigilante for CROs With AI and ML [presentation] Vidya Muthukumar source 18
PHUSE US 2022 SPACE - Launching GSK Biostatistics towards new horizons Eileen Ching source
presentation source		 10
PHUSE US 2022 Staying Ahead of the Curve: The Future Direction of Modernization of Statistical Analytics (MSA) [presentation] Peter Mesenbrink source 19
PHUSE US 2022 Trial Summary SDTM Domain Made Easy for Regulatory Submissions [presentation] Kishore Pothuri source 16
PHUSE EU 2021 DEEP Presentation and Launch? : New Era of Collaboration - DEEP Enables an Ecosystem Approach to Advance Digital Medicine [presentation] Bert Hartog,
Kai Langel		 source 30
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 Fingerprinting Your TFL Outputs to Monitor Changes Between Batch Runs [presentation] Pamphile Beaujean source
video		 20
PHUSE EU 2021 Incorporating Novel Real-world Evidence Across the Drug Development Continuum: Leveraging the Value of Digital Social Media [presentation] Nardin Farid,
Stephen Doogan		 source
video		 24
PHUSE EU 2021 New Starters Session: The Secret Sauce to Start in Our Industry [presentation] Amritpal Singh,
Lucie Bowden		 source 5
PHUSE EU 2021 New Starters Session: The Secret Sauce to Start in Our Industry [presentation] Amritpal Singh,
Lucie Bowden		 source 11
PHUSE EU 2021 R and SAS Working Together - DNR's Experience Moving to LSAF 5.3 [presentation] Paul Vervuren source
video		 17
PHUSE EU 2021 Real-time Analysis of Clinical Trial Data [presentation] Jem Chang,
Prasanna Murugesan		 source
video		 9
PHUSE EU 2021 Real-world Data, CDISC SDTM, HL7 FHIR and the Future of Regulatory Submissions [presentation] Jozef Aerts source
video		 17
PHUSE EU 2021 Software Demonstration: Unlocking Value from Structured Clinical Trial Data - Sponsored by Privacy Analytics [presentation] Thomasin Element source 18
PHUSE EU 2021 Standing Room Only: AR02: The Importance of Being Ernest - The Role of QTLs in QbD [presentation] Andrew Lawton source 19
PHUSE EU 2021 Standing Room Only: SA04: Diversity, Equity and Inclusion of Your Submission Package [presentation] Anne-Sophie Bekx source 19
PHUSE EU 2021 Study Designs Using FHIR - Schedule of Activities Exchange Using FHIR Resources [presentation] Andy Richardson source
video		 19
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 Artificial Intelligence (AI) Innovations in Clinical Research [poster] Sanjeeva Thalla source 1
PHUSE US 2021 Data Science Presentations: DSc01: How Automation Using Machine Learning Technology Can Overcome the Limitations of Double Programming [presentation] Hugh Donovan,
Ilan Carmeli		 source 18
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 From Digital Data to Decision Intelligence: Infrastructure and Algorithms Powering Automation in RBM and Data Review [presentation] Raj Indupuri source
video		 12
PHUSE US 2021 Interactive Visualization and Summarization of Toxicology Study Results Across Species, Routes and Durations Throughout a Drug Development Program Using R Shiny [presentation] Kevin Snyder,
Md Yousuf Ali		 source
video		 14
PHUSE US 2021 Is it ART? An Application of TransCelerate's MoA Framework for Assessing Accuracy, Reproducibility and Traceability in Novel Software Implementations [presentation] Michael S Rimler,
Tim Kuhn		 source 20
PHUSE US 2021 Leadership Presentations: LE06: One Sprint at a Time - Agile Transformation in Clinical Research [presentation] Aman Bahl,
Steve Benjamin		 source 17
PHUSE US 2021 Next Evolution Step(s) for Statistical Programmers: "Clinical Data Scientist" or "Clinical Data Analytics Engineer"? [presentation] Amar Mahidadia,
Sascha Ahrweiler		 source
video		 16
PHUSE US 2021 Patient Registries - New Gold Standard for Real World Data [presentation] Lavanya Peddibhotla,
Sivasankar Konda		 source
video		 14
PHUSE US 2021 Self-sufficient Exploration of Clinical Trial Events in Different Ways and in Different Contexts [presentation] Eva Kelty source
video		 15
PHUSE US 2021 Statistical Programming Team Contributions to Registrational Clinical Research Collaborations (rCRCs) [poster] Norihiko Oharu,
Yan Shen		 source 1
PHUSE US 2021 Using Natural Language Processing to Create Subject Safety Narratives [presentation] Frank Meloni,
Tim Willittes		 source
video		 8
PharmaSUG 2021 A TransCelerate Initiative - how can you modernize your statistical environment? Vincent J. Amoruccio,
Min Lee,
Daniel Woodie		 source 16
PharmaSUG 2021 An efficient method to review annotation and create bookmark for case report form (acrf.pdf) using SAS program, FDF files, excel and Javascript in Acrobat Chen-Jung Wu source 12
PharmaSUG 2021 Bookdown and Blogdown: Using R packages to document and communicate new processes to Clinical Programming Benjamin Straub source 11
PharmaSUG 2021 Containers You Can Count On: A Framework for Qualifying Community Container Images Eli Miller source 4
PharmaSUG 2021 Delight the Customer using agile transformation in Clinical Research Aman Bahl,
Steve Benjamin,
Hrideep Antony		 source 9
PharmaSUG 2021 Generating FDA-ready Submission Datasets directly from EHRs Jozef Aerts source 9
PharmaSUG 2021 How simulation will impact the future of Healthcare & Life Sciences. Pritesh Desai,
Allison Sealy,
Shawn Tedman,
Lois Wright,
Bahar Biller		 source 14
PharmaSUG 2021 Productionalizing Shiny Deployments Philip Bowsher,
Sean Lopp		 source 6
PharmaSUG 2021 Shiny App for Generating Data Dependency Flowchart in ADRG Simiao Ye,
Yilong Zhang		 source 8
PharmaSUG 2021 Virtual human organs in clinical trails Sumeet Subhedar source 3
PharmaSUG 2021 Why Data Scientists need leadership skills? Story of Cross-Value Chain Data Utilization Project Yura Suzuki,
Yuichi Koretaka,
Ryo Kiguchi,
Yoshitake Kitanishi		 source 8
PHUSE EU 2020 An Introduction to the Use of BigQuery for the Life Sciences [presentation] Claudio Garutti source
video		 14
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 Drug Safety and Efficacy - Smart Regulatory Solution [presentation] Haider Ali,
Rhim Suh Ngu'eh Shu		 source
video		 17
PHUSE EU 2020 Enhanced COVID-19 (SARS-COV-2) Detection - An Artificial Intelligence Approach [presentation] Muhammad Hamiz Ahmed,
Soundarya Palanisamy		 source
video		 37
PHUSE EU 2020 Guide to Electronic Submission of Pharmacometric Datasets and Analyses to the Regulatory Authorities [presentation] Pooja Kulkarni source
video		 17
PHUSE EU 2020 MI FOR MI, OR HOW TO HANDLE MISSING INFORMATION WITH MULTIPLE IMPUTATION Daria Shamaida source
video
presentation source		 8
PHUSE EU 2020 Patient Insights and Real-world Data from Social Media [presentation] Luisa Regenold,
Soundarya Palanisamy		 source
video		 28
PHUSE EU 2020 Power BI in Clinical Data Exploration: Powerful Visuals that Answer Relevant Questions Roxane Debrus source
video
presentation source		 11
PHUSE EU 2020 SDTM: Let's Read Outside the Bible [presentation] Sandra Latorre source
video		 23
PHUSE EU 2020 The TransCelerate Hackathon: Accelerating Development [presentation] Johannes Ulander source
video		 26
PHUSE EU 2020 Unlocking the Potential of Big Data in Clinical Research [presentation] Vishal Kapoor source
video		 15
PHUSE EU 2020 XAI: Interpretability of Artificial Intelligence to Ensure Ethics in Drug Development [presentation] Olivier Bouchard source
video		 13
SGF 2020 Statistical Programming in the Pharmaceutical Industry: Advancing and Accelerating Drug Development Harper Forbes source 10
SGF 2020 Transfer Learning for Mining Digital Phenotype by SAS Viya Satoki Fujita source 18
PharmaSUG 2020 Natural History Study - A Gateway to Treat Rare Disease Tabassum Ambia source 5
PharmaSUG 2020 You down to QC? Yeah, You know me! Vaughn Eason,
Jake Gallagher		 source 5
PHUSE US 2020 A Journey Through End to End Data Flow Marcin Makowski,
Stayce Murray		 source
presentation source		 12
PHUSE US 2020 An Approach to Dynamic Data Visualization with dplyr DT and Shiny Megan Kendellen,
Nicholas Masel		 source
presentation source		 11
PHUSE US 2020 Artificial Intelligence (AI)-enhanced Precision Medicine Drug Development Mohammad Afshar source 9
PHUSE US 2020 Be the Master for a Master Protocol Study Ke Xiao source
poster source		 8
PHUSE US 2020 Best Practice for Interactive Analysis for Decision-making: An update from PHUSE Data Visualization Project Xiangyun Wang,
Zachary Skrivanek		 source 11
PHUSE US 2020 CDISC 360: Using Biomedical Concept Metadata to Generate Case Report Forms and Dataset Definitions Samuel Hume source
presentation source		 13
PHUSE US 2020 Clarity Stack Clinical Technology - A Holistic View of Clinical Trial Operational Status and Patient Safety Data [presentation] Dirk Spruck,
Lisa Jamba		 source 10
PHUSE US 2020 Data Science Project (Educating for the Future Working Group) Aldir Medeiros Filho,
Sascha Ahrweiler		 source
presentation source		 10
PHUSE US 2020 Data Standards for eCOA in Clinical Trials Terek Peterson,
Franklin E. Menius		 source
presentation source		 6
PHUSE US 2020 Data Visualization for Medical Review Bharath Sunkavalli source
presentation source		 4
PHUSE US 2020 Design and Conduct of Clinical Trials: Past Present and Future. New Innovative Technology Methods George Obsekov source
presentation source		 12
PHUSE US 2020 Evolution of Clinical Data Disclosure and Transparency Sneha Paradkar source
presentation source		 8
PHUSE US 2020 FDA and PMDA Study Data Submission Distinctions Kiran Kumar Kundarapu,
Nancy Bauer		 source
poster source		 13
PHUSE US 2020 Getting e-Closer to Multi-Regional Clinical Trials Lily Ling,
Yuan Yuan Dong,
Yanhong Li		 source
presentation source		 5
PHUSE US 2020 Industry Experiences Submitting Standardized Study Data to Regulatory Authorities Janet Low,
Vincent Guo		 source
presentation source		 12
PHUSE US 2020 Integration of Biomarkers Data in Clinical Trials Prakash Dev source
presentation source		 5
PHUSE US 2020 Is R language reliable and efficient tool for programming SAS datasets or just art for art's sake? Piotr Podlewski source
presentation source		 9
PHUSE US 2020 Machine Learning-AI is the Future - What Now? Priyanka Adusumilli,
Priyank Patel		 source
poster source		 8
PHUSE US 2020 Managing Data Flow for Wearables, Apps and Sensors Mayur Tripathi,
Prashanth Jayadevamurthy		 source
presentation source		 4
PHUSE US 2020 Migrating to LSAF - The Danone Nutricia Research Journey Jean-Marc Ferran,
Paul Vervuren		 source
presentation source		 9
PHUSE US 2020 Open Source Technologies in Clinical Research Bruce Wienckowski,
Michael S Rimler		 source
presentation source		 7
PHUSE US 2020 Population PK Dataset: Basic Concepts and Challenges from the Perspective of a SAS Programmer Namrata Pokhrel source
presentation source		 12
PHUSE US 2020 Project Programmer @GSK...the Journey Continues! Eileen Ching,
Raghu Kumbharathi		 source
presentation source		 8
PHUSE US 2020 R & Python for Clinical Workflows Philip Bowsher source 13
PHUSE US 2020 Recommendations for GDPR Compliancy by the PHUSE Data Transparency Working Group GDPR Project Arlene Coleman,
Shannon Labout		 source
poster source		 3
PHUSE US 2020 Rerouting Your Risk-based Monitoring Strategy: Overcoming Implementation Roadblocks with New Technologies and Approaches Jonathan Andrus source
presentation source		 9
PHUSE US 2020 SPA - A catalyst for clinical protocol development Suhas Giriraj,
Ephicacy Lifescience		 source
presentation source		 5
PHUSE US 2020 Using Graph Technology for Metadata-driven Clinical Development Frederik Malfait source 6
PHUSE EU 2019 Addressing the Gap in Data Standards: Introducing the Aggregation Layer Claudio Garutti,
Marko Bomyer		 source
presentation source		 11
PHUSE EU 2019 Clearing the Fog Surrounding LOINC Jordan Bristow source
presentation source		 7
PHUSE EU 2019 Educating for the Future: Data Engineering Techniques Guy R. Garrett source
presentation source		 10
PHUSE EU 2019 GDPR: Risks and Recommendations from the PHUSE Data Transparency Working Shannon Labout,
Arlene Coleman		 source
presentation source		 7
PHUSE EU 2019 Integrated Data and Document Anonymisation for Efficient Data Sharing [presentation] Ali Dootson,
Cathal Gallagher		 source 27
PHUSE EU 2019 Migrating to LSAF - Danone Nutricia Research's Journey Paul Vervuren,
Jean-Marc Ferran		 source
presentation source		 9
PHUSE EU 2019 Onboarding a Junior Statistical Programmer in 10 Weeks: My Story, from University to First Analysis Delivery Pieter Coppens,
Annelies Van Zeveren		 source
presentation source		 6
PHUSE EU 2019 Our Industry: Technology-driven or Driven by Technology? Faheeza Rangunwala source
presentation source		 9
PHUSE EU 2019 Pharmacokinetic and Statistical Considerations in First-in-Human Clinical Trials Joanna Magielse source
presentation source		 4
PHUSE EU 2019 Processing big data from multiple sources Berber Snoeijer source
presentation source		 5
PHUSE EU 2019 R you ready for Simulo: a user-friendly clinical trial simulator Quentin Leirens,
SGS Exprimo,
Nicolas Luyckx,
SGS Exprimo,
Bruno Speder,
SGS Exprimo		 source
presentation source		 7
PHUSE EU 2019 Structured Clinical Development - Using a Digitized Study Design and Planning to Drive Process Automation Djenan Ganic source
presentation source		 7
PHUSE EU 2019 The Impact of AI, RWE, Precision Medicine and Mobile Health Technology on Streamlined Clinical Trials Stijn Rogiers,
Olivier Bouchard		 source
presentation source		 11
PHUSE EU 2019 The Promise of Wearable Technology in Clinical Trials: A Proof of Concept to Deliver it? Jennifer Bradford source
presentation source		 11
PHUSE EU 2019 Towards a Biomedical Concept Library: Creating and Sharing Biomedical Concepts David Iberson-Hurst source
presentation source		 7
PHUSE EU 2019 Use of FHIR in Clinical Research: From Electronic Medical Records to Analysis Jeffrey M. Abolafia,
Priya Gopal,
Samuel Hume		 source
presentation source		 12
PHUSE EU 2019 Utilising RWD and RWE: An Introduction to Core Concepts and Requirements Christopher C. Hurley,
Aditya Gadiko		 source
presentation source		 7
WUSS 2019 Root Cause Analysis Using Pinnacle 21 Validation Reports: How to Improve End-to-End Programming Process Aakar Shah,
Tracy Sherman		 source 13
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 Begin with the End of Validation: Adapting QbD Approach in Statistical Programming to Achieve Quality and Compliance Excellence Linghui Zhang source 8
PharmaSUG 2019 CBER Data Standards Update and BioCompute Progress Elaine Thompson source 27
PharmaSUG 2019 China NMPA (National Medical Products Administration) reform and new regulations/guidelines/requirements Yi Yang source 11
PharmaSUG 2019 Don't Just Rely on Processes; Support Local Subject Matter Expertise Deidre Kreifels,
Steven R. Kirby,
Mario Widel		 source 7
PharmaSUG 2019 Expediting Drug Approval: Real Time Oncology Review Pilot Program Laxmi Samhitha Bontha source 4
PharmaSUG 2019 Innovative Technologies utilization in 21st Novel Clinical Research programs towards Generation of Real World Data. Srinivasa Rao Mandava source 6
PharmaSUG 2019 Process optimization for efficient and smooth e-data submissions to both FDA and PMDA Eri Sakai,
Malla Reddy Boda,
Akari Kamitani,
Yoshitake Kitanishi		 source 13
PharmaSUG 2019 SDSP (Study Data Standardization Plan) Case Studies and Considerations Kiran Kumar Kundarapu source 8
PharmaSUG 2019 The Anatomy of Clinical Trials Data: A Beginner's Guide Venky Chakravarthy source 14
PharmaSUG 2019 This Paper focuses on CDISC Questionnaires, Ratings and Scales (QRS) supplements and types of FDA Clinical Outcome Assessments Shrishaila Patil source 10
SGF 2019 Make SAS Viya Realize Strategic Data Science - Data Governance, AI Platform and AI SAS Programmer Ryo Kiguchi,
Katsunari Hirano,
Yoshitake Kitanishi		 source 8
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 Analysis and Reporting Workbench (ARW) Demo Jenna Lo source
presentation source		 3
PHUSE US 2019 CDISC Blue Ribbon Commission Update to Our Community David Bobbitt source
presentation source		 4
PHUSE US 2019 CDISC in Phase I/II Studies: Case Studies in Adopting Standards Emily Woolley,
Amber Randall Scharp		 source
presentation source		 7
PHUSE US 2019 Delivery of Data Visualizations within GlaxoSmithKline Clinical Development and Partners via an ELD Model Jason Szewczyk source
presentation source		 5
PHUSE US 2019 Development of a Risk-based Monitoring (RBM) Visualization Application Interface Using JMP Scripting Dongsun Cao,
Bhargava Reddy		 source
presentation source		 13
PHUSE US 2019 Graphical Examination of PK Parameters Versus Dose-in-Dose Escalation Trials using SAS GTL Chiu Tsang,
Hima Bhatia		 source
poster source		 9
PHUSE US 2019 Harness the Power of Ontologies to Build Better Information Platforms Peter Tormay,
Anna Berg		 source
presentation source		 7
PHUSE US 2019 Implementing a Scalable Risk-based Monitoring Strategy Steve Young,
Erik Doffagne		 source
presentation source		 4
PHUSE US 2019 Interactive Monitoring of Hepatotoxicity Susan Duke source
presentation source		 10
PHUSE US 2019 Managing Complexity Towards Submission Johannes Ulander source
presentation source		 26
PHUSE US 2019 Metadata-driven Automation in Drug Research Hanming Tu,
Zhongping Lin		 source
presentation source		 13
PHUSE US 2019 New Drug Development Paradigm [presentation] Francis Kendall,
Cytel		 source 33
PHUSE US 2019 R Markdown for Reproducible Research Cole Arendt source
presentation source		 15
PHUSE US 2019 SDSP (Study Data Standardization Plan) Case Studies and Considerations Kiran Kumar Kundarapu,
Nicole Gallegos		 source
poster source		 6
PHUSE US 2019 Simulo - A User-friendly Platform for Model-based Simulations Nicolas Luyckx,
Quentin Leirens		 source
presentation source		 7
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 Power of Sharing Clinical Data: Real Projects with Real Impacts David Handelsman source
presentation source		 6
PHUSE US 2019 Use of FHIR in Clinical Research: From Electronic Medical Records to Analysis Priya Gopal source
presentation source		 12
PHUSE US 2019 Using Study Metrics to Monitor Several Aspects of Clinical Studies Virtually Real Time Julio Ruiz source
presentation source		 6
PHUSE EU 2018 AstraZeneca Early Clinical Biometrics Journey into Integrated Clinical Data Environment Ruhul Amin,
Per-Arne Stahl		 source
presentation source		 12
PHUSE EU 2018 CDISC SDTM Data Automation Tool Brinitha Sathyabhama source
presentation source		 6
PHUSE EU 2018 Data Engineering Project (Educating for the Future PHUSE Working Group) Guy R. Garrett,
Bev Hayes		 source
presentation source		 14
PHUSE EU 2018 Data Transparency - Breaking Down Data Silos for Improved Insight Peter Tormay,
Anna Berg		 source
presentation source		 8
PHUSE EU 2018 iGET it! Downloading Data from a Centralised Repository Using PROC HTTP Neville Cope source
presentation source		 7
PHUSE EU 2018 Implementation of a Metadata-based Approach to Statistical Planning, Analysis and Reporting Frank Freischlager,
Hanspeter Schnitzer		 source
presentation source		 7
PHUSE EU 2018 Is it Possible to Make a Global CDISC Submission? Marianne Carames source
presentation source		 2
PHUSE EU 2018 Navigating the Mountains and Valleys of Resource Demand: A Roadmap for the Future Lucy Hoch,
Yvonne Jangvik		 source
poster source		 7
PHUSE EU 2018 SAS Life Science Analytical Framework (LSAF) in a Nutritional Clinical Research Setting Mickaël Hartweg,
Justine Morlet		 source
presentation source		 7
PHUSE EU 2018 Structured and Standardised Study Definition Drives Early Study Set-up for Added Business Benefits Djenan Ganic,
Tanja Petrowitsch		 source
presentation source		 11
PHUSE EU 2018 The 5 Rs of Innovative Digital Technologies Anna Hedman,
Charlotte Lomberg		 source
poster 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
MWSUG 2018 Toward Adoption of Agile Software Development in Clinical Trials Troy Martin Hughes 7
WUSS 2018 CDISC in Phase I/II Studies: Approaches to adopting standards for CSR deliverables Emily Woolley,
Amber Randall		 source 9
PHUSE US 2018 Alexa for Clinical Research Chris Decker source
presentation source		 6
PHUSE US 2018 Evaluating how Blockchain can Transform the Pharmaceutical and Healthcare Industry Disa Lee Choun,
Jim Nasr		 source
presentation source		 9
PHUSE US 2018 FDA Experience with Emerging Genomics Technologies [presentation] Weida Tong source 16
PHUSE US 2018 Implementing an Metadata Repository Solution - A User Story Barrie Nelson,
Wade Fairbanks		 source
presentation source		 5
PHUSE US 2018 Making PK Analysis Easier: The New ADaM Data Standard ADNCA Peter Schaefer source
presentation source		 6
PHUSE US 2018 Mine the Gap: How the Role of Data Scientist Fills a Need in the Pharmaceutical Industry Michael S Rimler,
Jorine Putter		 source
presentation source		 8
PHUSE US 2018 PHUSE Working Groups - Now & Nex Chris Price,
Scott A. Bahlavooni		 source
poster source		 7
PHUSE US 2018 Registry/Observational Studies: Study Designs Data Sources and Key Steps in Designing Such Studies Anupama Sheoran source
presentation source		 6
PHUSE US 2018 SDTM and SEND: An Integrated View and Approach Veena Nataraj,
Cheryl Riel		 source
presentation source		 11
PHUSE US 2018 Supporting a Data Review and Visualization Application with SDTM Deepika Sunkara,
Jagadish Dhanraj		 source
presentation source		 6
PHUSE US 2018 The Untapped Potential of the Protocol Representation Model Jeffrey M. Abolafia,
Frank C. DiIorio		 source
presentation source		 10
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
PHUSE US 2018 Using a Waiver Process as a Change-Control Tool from ADaM Standards Governance Karin LaPann source
presentation source		 6
PharmaSUG 2018 Advanced Clinical Graphs using Axis Tables Sanjay N. Matange source 11
PharmaSUG 2018 AGING MAN_AGEMENT or millennial TECH_AGEMENT - road ahead for organizations Charan Kumar K J source 12
PharmaSUG 2018 Compare Pharmacokinetic Data Submission Processes in CDISC Environment Xiaopeng Li,
Shallabh Mehta,
Edward Elam		 source 7
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 Mind Over Matter: Building an Army of Passionate Soldiers Dedicated to Saving Patients' Lives Shefalica Chand source 10
PharmaSUG 2018 Preventing premature unblinding in PK/PD related studies Debbie Sisco,
Alice Zong		 source 11
PharmaSUG 2018 Programming Support for Anti-Drug Antibody Pharmacokinetics in Therapeutic Protein Drug Development Linghui Zhang,
Jiannan Kang		 source 11
PharmaSUG 2018 Using JMP Scripting Language (JSL) to create an application interface for automated analysis of Lab Data in Clinical Trial Dongsun Cao source 11
PharmaSUG 2018 Why organizations need MDR systems to manage metadata? Abhinav Jain source 7
SGF 2018 Advanced Graphs Using Axis Tables Sanjay N. Matange source 12
SGF 2018 The Anatomy of Clinical Trials Data: A Beginner's Guide Venky Chakravarthy source 14
SESUG 2017 Extracting Clinical Research Data from OnCore and Preparing it for Statistical Analysis in SAS Chang Xu,
Dominic T. Moore,
Allison M. Deal		 source 13
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 Connected Trials Abi Velurethu source
presentation source		 10
PHUSE EU 2017 Devices Big Data and Real World Evidence Mike Collinson source
presentation source		 7
PHUSE EU 2017 Extension Studies - CDISC Submission Challengesand Scenarios Arvind Sri Krishna Mani,
Deepak Anathan		 source
presentation source		 3
PHUSE EU 2017 Git with It and Version Control! Carrie Dundas-Lucca,
Ivan Gomez		 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
PHUSE EU 2017 How to Fit Longitudinal Data with Proc MCMC Maud Henion source
presentation source		 16
PHUSE EU 2017 Industry Standards - What Else Exists Beside CDISC Joerg Dillert source
presentation source		 8
PHUSE EU 2017 PHUSE is Moving Cloud Adoption Forward in Life Sciences Tony Hewer source
presentation source		 6
PHUSE EU 2017 Putting Sisyphus Out of a Job, Making Health Care Research a Reality [presentation] Geoff Low source 26
PHUSE EU 2017 The Untapped Potential of the Protocol Representation Model Jeffrey M. Abolafia,
Frank C. DiIorio		 source
presentation source		 10
PHUSE EU 2017 Topology-based Clinical Data Mining: Identifying Hidden Patterns in Clinical Datasets Sergey Glushakov source
presentation source		 18
WUSS 2017 A Critique of Implementing the Submission Data Tabulation Model (SDTM) for Drugs and Medical Devices Carey G. Smoak source 16
PharmaSUG 2017 A Critique of Implementing the Submission Data Tabulation Model (SDTM) for Drugs and Medical Devices Carey G. Smoak source 16
PharmaSUG 2017 Ahead of the Curve: Leading with Industry Data Requirements Maria Dalton,
Nancy Haeusser		 source 17
PharmaSUG 2017 The Road Not Taken: SAS for Pharmacometrics Vishak Subramoney,
Sree Harsha Sreerama Reddy		 source 4
PharmaSUG 2017 The Untapped Potential of the Protocol Representation Model Frank C. DiIorio,
Jeffrey M. Abolafia		 source 10
PharmaSUG 2017 Topology-based Clinical Data Mining for Discovery of Hidden Patterns in Multidimensional Data Sergey Glushakov,
Iryna Kotenko,
Andrey Rekalo		 source 20
PharmaSUG 2017 Update on Data Standards Ronald Fitzmartin source 25
PharmaSUG 2017 Usage of Pinnacle 21 Community Toolset 2.x.x for Clinical Programmers Sergiy Sirichenko,
Michael DiGiantomasso		 source 23
PharmaSUG 2017 What Makes a Candidate Stand Out? Edward Slezinger source 3
PharmaSUG 2017 Writing Efficient Queries in SAS Using PROC SQL with Teradata Mina Chen source 5
SGF 2017 A Critique of Implementing the Study Data Tabulation Model (SDTM) for Drugs and Medical Devices Carey G. Smoak source 16
SGF 2017 Creating Daily Rolling 6-Month Average and Cumulative Enrollment Graphs Using PROC EXPAND and INTNX Susan Schleede source 10
PHUSE EU 2016 An Update from the PHUSE Working Group on Cloud Adoption in the Regulated Life Sciences Industry Tony Hewer source
presentation source		 33
PHUSE EU 2016 Data Sharing 3 Years on - From Baby to Toddler... Katherine Tucker source
presentation source		 10
PHUSE EU 2016 How a Metadata Repository Enables Dynamism and Automation in SDTM-like SAS Dataset Generation Judith Goud,
Akana Shetty		 source
presentation source		 7
PHUSE EU 2016 How to Enjoy Working in Virtual Teams Petra Auclair,
Antje Rossmanith		 source
presentation source		 4
PHUSE EU 2016 Planning for Data Reporting Processes for Submission: Key Considerations Parag Shiralkar source
presentation source		 2
PHUSE EU 2016 Protocol Representation: The Forgotten CDISC Model Jeffrey M. Abolafia,
Frank C. DiIorio		 source
presentation source		 10
PHUSE EU 2016 The Hardships of Finding your Way in Biometrics Evi Creebsburg source 4
PHUSE EU 2016 The Tortoise Versus the Hare - And the Winner is... Meena Rahman,
Rebecca Leivers		 source
presentation source		 4
PHUSE EU 2016 To Create Define-XML Using - XML and the OpenCDISC Validator [presentation] Murali Neela source 17
WUSS 2016 An Array of Fun: Macro Variable Arrays Kalina Wong,
Sarah Short		 source 5
PharmaSUG 2016 Are You Thinking About Becoming an Independent Contractor? Things to Consider as you Plan for Your New Entrepreneurship Kathy Bradrick,
Dawn Edgerton		 source 4
PharmaSUG 2016 Considerations and Conventions within the Therapeutic Area User Guides (TAUGs) Jerry Salyers,
Kristin Kelly,
Fred Wood		 source 8
PharmaSUG 2016 Enough of Clinical ... Let's talk Pre-Clinical! Arun Raj Vidhyadharan,
Sunil Mohan Jairath		 source 5
PharmaSUG 2016 Getting Clouds Moving across the Pacific - a case study on working with a Chinese CRO on SAS Drug Development Chen Shi source 4
PharmaSUG 2016 Importance of Niche Provider for Successful NDA Submission: Rescue Case Study Aparna Poona,
Bhavin Busa,
Tim Southwick		 source 9
PharmaSUG 2016 Journey from the student to the full-time programmer Viktoriia Vasylenko source 4
PharmaSUG 2016 Programming Support for Exposure-Response Analysis in Oncology Drug Development Peter Lu,
Hong Yan		 source 8
PharmaSUG 2016 Scrambled Data - A Population PK/PD Programming Solution Sharmeen Reza source 8
PharmaSUG 2016 Strategic Considerations for CDISC Implementation Amber Randall,
William Coar		 source 6
PharmaSUG 2016 Transforming Biomarker Data into an SDTM based Dataset Kiran Cherukuri source 7
PharmaSUG 2016 Usage of Pinnacle 21 Community Toolset 2.1.1 for Clinical Programmers Sergiy Sirichenko,
Michael DiGiantomasso,
Travis Collopy		 source 19
SGF 2016 Careers in Biotatistics and Clinical SAS Programming: An Overview for the Uninitiated Justina M. Flavin source 5
PHUSE EU 2015 A Simple and Novel Approach for the Assessment of Clinical Pharmacokinetics (Fast-track PK Analysis) [presentation] Ramanatha Saralaya,
Nand Kishore Rawat		 source 12
PHUSE EU 2015 A StAR is Born: AstraZeneca/Quintiles Partnering for Success Alison Dobson,
Alex Brink		 source
presentation source		 6
PHUSE EU 2015 Data Encoding:All Characters for All Countries Donna Dutton source
presentation source		 12
PHUSE EU 2015 Data Scientist - What It Is (Not) Michaela Jahn source
presentation source		 4
PHUSE EU 2015 Metadata Snapshots: How SAS Drug Development API Macros Can Help Melissa R. Martinez source
presentation source		 12
PHUSE EU 2015 PHUSE De-identification Working Group: Providing identification Standards to CDISC Data Models Jean-Marc Ferran,
Khaled El Eman		 source
presentation source		 13
PHUSE EU 2015 Preparing and Utilising Claims and Electronic Medical Records Data for Clinical Research Laurie Rose source
presentation source		 5
PHUSE EU 2015 Programming Strategically for PK/PD Data Grace Lu source
presentation source		 8
PHUSE EU 2015 Similarities and Differences in Statistical Programming Among CROs and Pharmaceutical Industries Mark Matthews source
presentation source		 7
PHUSE EU 2015 The AQSCI Method Behind CRO Evaluation and Application to Pharmaceutical Company Needs Roy Ward,
James Gallagher		 source
presentation source		 8
PHUSE EU 2015 The Evolution of Computing in Clinical Research: Past, Present and Future Mark Weadon source
presentation source		 6
PHUSE EU 2015 The Vision of Clinical Data Science - Where will we be in 2025? [presentation] Sam Warden,
Chris Price		 source 17
PHUSE EU 2015 Unleashing the Analyst: Establishing a Department of Dynamic Real-world Data Science (RWD-S) Analysts who are able to Partner, Influence and Drive the Generation of Real-world Evidence Ryan Copping,
Robert Walls		 source
presentation source		 28
PHUSE EU 2015 Using SAS Graphics to Help with Decision-making in Early Clinical Development Sinela Hadzovic source
presentation source		 3
PHUSE EU 2015 Work Harder or Work Smarter? Colin Brown source
presentation source		 4
WUSS 2015 No Regrets: Hiring for the Long Term in Statistical Programming Chris Moriak,
Graham Wilson,
Elizabeth Meeson		 source 7
PharmaSUG CN 2015 Clinical trials optimization: Monte Carlo Simulation modeling and SAS applications Ye Meng 5
PharmaSUG CN 2015 SAS End-to-End solutions in Clinical Trial Emma Liu 17
PharmaSUG 2015 A New Era: Open access to clinical Trial Data - A case study Aruna Kumari Panchumarthi,
Jacques Lanoue		 source 6
PharmaSUG 2015 Advantages and Disadvantages of Two Commonly Used CRO Resourcing Models in the Pharmaceutical SAS Programming Environment Ying (Evelyn) Guo,
Mark Matthews		 source 7
PharmaSUG 2015 Automating Clinical Trial Reports with ODS ExcelXP Tagset John R. O'Leary source 8
PharmaSUG 2015 CRO, TLF, SOP? OMG!: A Beginner's Guide to the Clinical Research Organization Mandy Bowen,
Otis Evans,
Stephen Terry		 source 7
PharmaSUG 2015 Development of a Clinical SAS University Training Program in Eastern Europe Erfan Pirbhai,
Sergey Glushakov		 source 7
PharmaSUG 2015 Getting Rid of Bloated Data in FDA Submissions Ben E. Bocchicchio,
Frank L. Roediger		 source 8
PharmaSUG 2015 Growing Needs in Drug Industry for NONMEM Programmers Using SAS Sharmeen Reza source 11
PharmaSUG 2015 No Regrets: Hiring for the Long Term in Statistical Programming Chris Moriak,
Graham Wilson,
Elizabeth Meeson		 source 7
PharmaSUG 2015 PhUSE De-Identification Working Group: Providing De-Identification Standards to CDISC Data Models Jean-Marc Ferran,
Jacques Lanoue		 source 8
PharmaSUG 2015 The Disposition Table: Make it Easy Endri Endri,
Benedikt Trenggono		 source 10
PharmaSUG 2015 Toward Adoption of Agile Software Development in Clinical Trials Troy Martin Hughes source 7
PharmaSUG 2015 Usage of OpenCDISC Community Toolset 2.0 for Clinical Programmers Sergiy Sirichenko,
Michael DiGiantomasso,
Travis Collopy		 source 19
PharmaSUG 2015 Where are the SAS Jobs? Beth Ward,
Chelsea Jackson		 source 3
PHUSE EU 2014 A Day in the Life of a Data Sharing Specialist [presentation] Kelly Mewes source 29
PHUSE EU 2014 A Vision for the Future: Core Competencies for Statisticians and Programmers [presentation] James R. Johnson source 26
PHUSE EU 2014 Automated SDTM Creation and Discrepancy Detection Jobs: The Numbers Tell the Tale Joris De Bondt source
presentation source		 2
PHUSE EU 2014 Biomarker as Essential Part of Clinical Development Renuka Chinthapally source
presentation source		 7
PHUSE EU 2014 Change Management - An ICON Approach and Case Study Anagha Pradhan source
presentation source		 4
PHUSE EU 2014 Managing the Change - Evolving Statistical Programmers to Clinical Data Scientists Sascha Ahrweiler source
presentation source		 10
PHUSE EU 2014 Metadata, Study Standards, Interoperability: Key Concepts Toward Compliance to FDA Guidance Isabelle de Zegher source
presentation source		 3
PHUSE EU 2014 Risk based monitoring using integrated clinical development platform Authors Sita Rama Swamy Peddiboyina,
Shailesh Vijay Joshi		 source
presentation source		 9
PHUSE EU 2014 Spotfire for Clinical and Translational Medicine Gerard Conway source 3
PHUSE EU 2014 Statistics and Computing for Health A 10-year Bachelor of Science in South Brittany [presentation] Jean-Francoius Petiot,
Cedric Frambour		 source 17
PHUSE EU 2014 Submitting Summary Level Site Data: Overview, Implementation and Case Studies Robert F. Woolson,
Jeffrey M. Abolafia,
Ben Vaughn		 source
presentation source		 9
PHUSE EU 2014 Successfully Embracing Challenges to CDISC Standards [presentation] Elke Sennewald source 30
PHUSE EU 2014 Technology Trends with the Potential to Change Clinical Development Christopher R. Olinger source
presentation source		 5
PHUSE EU 2014 The On-Going Evolutionary Changes of our Industry [presentation] Christian Mueller source 34
PHUSE EU 2014 Update on Regulatory Guidance: Data Standardisation Planning for Clinical Development Programs James R. Johnson source
presentation source		 10
PHUSE EU 2014 Using CDISC Validation Tools in a Validated Hosted Environment Sandeep Juneja source
presentation source		 5
PHUSE EU 2014 What Makes one Project Successful and Another Stressful? Colin Brown source
presentation source		 5
PharmaSUG CN 2014 Design and Construct Efficacy Analysis Datasets in Later Phase Oncology Study Huadan Li,
Changhong Shi		 9
WUSS 2014 Careers in Biostatistics and Clinical SAS Programming: An Overview for the Uninitiated Justina M. Flavin source 5
PharmaSUG 2014 Automatic Access Control via SAS: More Efficient and Smart Yuichi Koretaka,
Masakazu Fujiwara,
Yuki Yoshida,
Yoshitake Kitanishi		 source 10
PharmaSUG 2014 Careers in Biostatistics and Clinical SAS Programming: An Overview for the Uninitiated Justina M. Flavin source 5
PharmaSUG 2014 Demystify "Ten years of pharma programming experience required" - What hiring managers actually look for Peng Yang source 3
PharmaSUG 2014 Distance Management: how to lead a team of SAS users who sit half a world away Max Cherny source 4
PharmaSUG 2014 Evaluating the benefits of JMP for SAS programmers Xiaopeng Li,
Chun Feng,
Nancy Wang		 source 9
PharmaSUG 2014 Inserting MS Word Document into RTF Output and Creating Customized Table of Contents Using SAS and VBA Macro Haining Li,
Merit E. Cudkowicz,
Hong Yu		 source 6
PharmaSUG 2014 Moving to SAS Drug Development 4 Magnus Mengelbier source 17
PharmaSUG 2014 Pick Me, Pick Me Deloris Jones,
Richard Harbin,
Monique Gainey		 source 4
PharmaSUG 2014 Round Trip Ticket - Using the Define.xml file to Send and Receive your Study Specifications Julie A. Maddox source 10
PharmaSUG 2014 Was Dorothy Right: Is There No Place Like Home? Kjersten Offenbecker source 6
SGF 2014 Bayesian Framework in Early Phase Drug Development with SAS Examples Howard Liang source 4
SGF 2014 Empowering Clinical Research Staff with SAS Enterprise Guide Christopher W. Schacherer source 20
WUSS 2013 Building a Controlled Statistical Programming Environment Wayne F. Woo source 10
WUSS 2013 The Poor Man's Program Metadata Extractor Joe Perry source 8
PHUSE EU 2013 A How-To Guide for Extending Controlled Terminology Using SAS Clinical Data Integration [presentation] Melissa R. Martinez source 71
PHUSE EU 2013 An Integrated Platform for Standards Management and Study Conduct - Managing Efficiently your Standards [presentation] Ine Felsenstein,
Jasmine Kestemont		 source 29
PHUSE EU 2013 Developing an Integrated Platform, Getting the Best out of Several Technologies [presentation] Jean-Marc Ferran,
Bart Van Win		 source 23
PHUSE EU 2013 EDC Integration [presentation] Rob Jongen source 21
PHUSE EU 2013 Evolving Regulatory Guidance on the Submission of Standardised Data [presentation] James R. Johnson source 25
PHUSE EU 2013 My Big Data Experience - Getting my Feet Wet in the PUddle and Still Treading Water 2 Years Later Robert Walls source
presentation source		 10
PHUSE EU 2013 My First QlikView Application "CTI" [presentation] Anthony Caudard source 12
PHUSE EU 2013 Posch-Bauer Seamless Test with SAS Antonio Nieto,
Javier Gómez		 source
presentation source		 4
PHUSE EU 2013 Round Trip Ticket - Using the Define.xml file to Send and Receive your Study Specifications Julie A. Maddox source
presentation source		 10
PHUSE EU 2013 Spotfire for Statisticians and Statistical Programmers [presentation] Alistair Dootson,
Mark Demesmaeker		 source 17
PHUSE EU 2013 Standard Protocols Using Guided Navigation [presentation] Michaela Jahn source 15
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 Visual Approaches for Safety Analysis and Review of Clinical Trials [presentation] Valérie Nedbal source 34
MWSUG 2013 An Efficient Approach to Automatically Convert Multiple Text Files (.TXT) to Rich Text Format Files (.RTF) Using SAS Xingxing Wu,
Jyoti N. Rayamajhi		 6
MWSUG 2013 Power Trip: A Road Map of PROC POWER Melissa Plets,
Julie Strominger		 4
PharmaSUG 2013 A GUI-Based Utility Macro for Creating a Version Controlled Project Directory Structure and Copying in Standard Tools and Template Files Hisham Madi,
Anna Maeser,
Michael Zichy		 source 12
PharmaSUG 2013 Deployment of SAS Programming Contract Staff: Pathway to Sinkhole or Best Strategy for Programming Division? Parag Shiralkar source 5
PharmaSUG 2013 From Standards that Cost To Standards that Save: Cost Effective Standards Implementation Jeffrey M. Abolafia,
Frank C. DiIorio		 source 9
PharmaSUG 2013 How to make SAS Drug Development more efficient Xiaopeng Li,
Chun Feng,
Peng Chai		 source 6
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 Modern SAS Programming: Using SAS Grid Manager and Enterprise Guide in a Global Pharmaceutical Environment David Edwards,
Gregory S. Barnes Nelson,
Susan Wang		 source 14
PharmaSUG 2013 Probability Based Criteria in Early Phase Drug Development Howard Liang source 5
PharmaSUG 2013 SAS 9.3: Better graphs, Easier lives for SAS programmers, PK scientists and pharmacometricians Alice Zong source 8
PharmaSUG 2013 Some Strategies for Validating Your Data before Submission Frank L. Roediger,
Sandeep Juneja		 source 8
PharmaSUG 2013 The Challenges and Opportunities for SAS Statistical Programmers in Two Commonly Used CRO Resourcing Models Mark Matthews,
R. Mouly Satyavarapu		 source 6
PharmaSUG 2013 Using the SAS Clinical Standards Toolkit 1.5 to Import CDISC ODM Files Lex Jansen source 28
PharmaSUG 2013 Using Workflows and Metadata Information to Standardize Business Processes in Pharmaceutical Programming Peng Yang,
Wei Liu,
Julie A. Maddox		 source 9
SGF 2013 Introducing and Producing Thunderstorm or Rain-drop Scatter Plots Using the SAS/GRAPH Annotate Facility Charlie Liu source 13
SGF 2013 Modern SAS Programming: Using SAS Grid Manager and SAS Enterprise Guide in a Global Pharmaceutical Environment David Edwards,
Gregory S. Barnes Nelson		 source 14
SGF 2013 Statistical Graphics for Clinical Research Using ODS Graphics Designer Wei Cheng source 12
NESUG 2012 Applying Business Analytics to Optimize Clinical Research Operations David Handelsman 8
PHUSE EU 2012 Clinical Reference Library: Metadata and Standards Management in a Single Tool [presentation] Jonathan Peachey,
Colin Sprink		 source 12
PHUSE EU 2012 Cost Effective Standards Implementation: A New Paradigm for the Drug Development Life Cycle Jeff Abolafio,
Frank C. DiIorio		 source
presentation source		 9
PHUSE EU 2012 Real-World Application of the Protocol Representations Model Joshua Pines,
Michelle Marlborough		 source
presentation source		 1
PHUSE EU 2012 SAS Drug Development 4.1 - Clinical Programming and Workflow Mark Weadon,
Mark Lambrecht		 source
presentation source		 8
PHUSE EU 2012 Spotting DILI for FDA Submission Nicola Tambascia,
Sven Greiner		 source
presentation source		 7
PHUSE EU 2012 The 3 Year Obsession: Length of Experiences the Sole Determinant of Competence? Meghana Bhagwat,
Manjusha Gode		 source
presentation source		 9
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
PHUSE EU 2012 Using Workflows to Standardize Business Processes and Best Practices in Pharmaceutical Programming Mark Lambrecht,
Julie A. Maddox		 source
presentation source		 7
SESUG 2012 A GUI-Based Utility Macro for Creating a Version Controlled Project Directory Structure and Copying in Standard Tools and Template Files Hisham Madi source 12
PharmaSUG CN 2012 Clinical Review on iPad with DEFINE.XML Sy J. Truong 10
PharmaSUG 2012 Creating Analysis Data Marts from SDTM Warehouses Frank L. Roediger source 9
PharmaSUG 2012 Export SAS Data to Excel in SAS Drug Development Chun Feng,
Xiaopeng Li		 source 10
PharmaSUG 2012 Risk Evaluation and Mitigation Strategies (REMS) and How They Impact Biostatistics and Statistical Programming Groups Arthur Collins source 4
PharmaSUG 2012 Statistical Graphics for Clinical Research Using ODS Graphics Designer Wei Cheng source 23
PharmaSUG 2012 Using File Modification Date Comparisons to Alert Study Teams of Potential SAS Program Revisions between Shared Folders Stephen Hunt,
Brian P. Fairfield-Carter		 source 6
SGF 2012 Applying Business Analytics to Optimize Clinical Research Operations David Handelsman source 8
SGF 2012 Sharing SAS programs between PC Server and SAS Drug Development Magnus Mengelbier source 7
WUSS 2011 Analyze This? Supporting Clinical Decisions Graphically When Not Enough Data is Available A Study Case: Challenges in NCI CTCAE Version 4 Grading Sheila Dayog source 4
WUSS 2011 Clinical Data Review on iPad with DEFINE.XML Sy J. Truong source 10
WUSS 2011 Statistical Graphics for Clinical Research Using ODS Graphics Designer Wei Cheng source 23
PHUSE EU 2011 A Career in the Pharmaceutical Industry James McDermott source
presentation source		 10
PHUSE EU 2011 Analysis and Reporting Toolset (A&RT): Lessons learned on how to develop a system with an external partner David Smith source
presentation source		 9
PHUSE EU 2011 Challengers Facing the Programmer in Observational Research Laurence Carpenter source
presentation source		 4
PHUSE EU 2011 Ensuring Compliant and Consistent Data Mappings for SDTM-based Studies - an ICON Approach Jennie McGuirk,
Steven Thacker		 source
presentation source		 16
PHUSE EU 2011 How do we ensure the programmer we have today will meet the business needs of tomorrow? Christine Leigh,
Karen Rowe		 source
presentation source		 8
PHUSE EU 2011 Know Your Sources - Decoding Inputs/Outputs of any SAS Program Sandeep Juneja source
presentation source		 5
PHUSE EU 2011 Managing Telecommuters and Global Virtual Teams Syamala Schoemperlen source
presentation source		 6
PHUSE EU 2011 New Starter Models for Pharmaceutical companies and Clinical Research Organisations (CROs) Lovemore Gakava source
presentation source		 4
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
PHUSE EU 2011 Sharing SAS programs between PC Server and SAS Drug Development Magnus Mengelbier source
presentation source		 7
PHUSE EU 2011 State of the union: what does the future hold for statistical programming in Europe [presentation] Leo Valmas source 28
PHUSE EU 2011 Using the SAS Clinical Standards Toolkit to work with the CDISC ODM model Lex Jansen source
presentation source		 20
PHUSE EU 2011 Writing standard programs your people will use and love! Jean-Marc Ferran source
presentation source		 8
MWSUG 2011 Optimizing Clinical Research Operations with Business Analytics David Handelsman 6
MWSUG 2011 Tracking Metadata within SAS Drug Development Using SDDPARMS Bradford J. Danner,
Matthew J. Wiedel,
Katrina E. Canonizado		 7
PharmaSUG 2011 A Non-Invasive Macro to Track Submission Metadata in SAS Drug Development Katrina E. Canonizado,
Bradford J. Danner,
Matthew J. Wiedel		 source 8
PharmaSUG 2011 Epidemiology in Drug Development Catherine Sigler,
Annette Stemhagen		 source 3
PharmaSUG 2011 SAS Drug Development Program Portability Ben E. Bocchicchio,
Nancy Cole		 source 9
PharmaSUG 2011 Similarities and Differences in SAS Programming Among CRO and Pharmaceutical Industries Sandra Minjoe,
Mark Matthews		 source 6
PharmaSUG 2011 Tracking Metadata within SAS Drug Development Using SDDPARMS Bradford J. Danner,
Matthew J. Wiedel,
Katrina E. Canonizado		 source 7
PharmaSUG 2011 Using SAS for Modeling and Simulation in Drug Development - A Review and Assessment of Some Available Tools Melvin S. Munsaka,
Michael Carniello		 source 10
SGF 2011 A Non-Invasive Macro to Track Submission Metadata in SAS Drug Development Katrina E. Canonizado,
Bradford J. Danner,
Matthew J. Wiedel		 source 8
SGF 2011 Achieving Efficiencies Using SAS Drug Development Aik Hoe Seah source 12
SGF 2011 Optimizing Clinical Research Operations with Business Analytics David Handelsman source 6
SGF 2011 State of the Union: The Crossroads of CDISC Standards and SAS Supporting Role Michael J. Molter,
Chris Decker		 source 14
NESUG 2010 A Few Quick and Efficient Ways to Compare Data Aileen D. Bennett 6
NESUG 2010 The Nitty-Gritty of FDA Electronic Submission: A Programmer's Perspective Sandeep N. Beniwal 9
NESUG 2010 The Past, Present, and Future of Clinical Data Standards Chris Decker 10
NESUG 2010 The SAS Programming Experience in the SAS Drug Development (SAS DD) Environment - Comparing with the Regular SAS Programming Environment Amos Shu 3
WUSS 2010 Essential Project Management Reports in Clinical Development Nalin Tikoo source 6
WUSS 2010 Patient Profile Reports on iPhone and iPad Sy J. Truong source 7
PHUSE EU 2010 An Open Source Reporting System for Life Sciences [presentation] Magnus Mengelbier source 32
PHUSE EU 2010 Assessing Applications Training Edel Hogan source
presentation source		 5
PHUSE EU 2010 Challenges of Clinical projects shared between Pharma Companies [presentation] Oliver LeConte source 27
PHUSE EU 2010 Defining "Compliance" for Analysis Data Chris Decker,
Randall Austin		 source
presentation source		 7
PHUSE EU 2010 EG as an IDE, how PC is that? [presentation] John Moone source 28
PHUSE EU 2010 From Data Capture to Decision Making Innovation through Standardization Michaela Jahn,
Stephan Laage-Witt		 source 5
PHUSE EU 2010 Interactive Clinical Data Review for Safety Assesment and Trial Operations Management Michael O'Connell source
presentation source		 13
PHUSE EU 2010 Lean Six Sigma:Measure and Improve [poster] Jinesh Patel source 1
PHUSE EU 2010 Modeling and Simulation: challenges for the clinical programmer and for the group leader [presentation] Vincent Buchheit source 18
PHUSE EU 2010 New CDISC migration strategies and tools: determining the best approach and employing automated data mapping [presentation] Michael Weitz,
Lauren Spiess		 source 29
PHUSE EU 2010 Qualities of a Project Manager Jon-Paul Mewes source
presentation source		 6
PHUSE EU 2010 Risk Radar for the Outsourcing of Clinical Trials: The Best Guide for Success Randy Ramin-Wright,
Raffael Jovine		 source
presentation source		 12
PHUSE EU 2010 SAS Drug Development Program Portability Ben E. Bocchicchio,
James McDermott		 source
presentation source		 9
PHUSE EU 2010 Statistical Graphics for Review and Reporting in Clinical Development Kerstin Pietzko,
Michael O'Connell		 source
poster source		 12
PHUSE EU 2010 The Challenges of Implementing New Technology on the Business Process Chris Decker source
presentation source		 11
PHUSE EU 2010 The Innovative Medicines Initiative Knowledge Management [presentation] Ann Marie Martin source 50
PHUSE EU 2010 Using web service technologies for incremental, real-time transfers Andrew Newbigging source 11
PharmaSUG 2010 Analytics in the Converging Health and Life Sciences Industries: The Catalyst for the Next Generation of Healthcare Matt Gross 15
PharmaSUG 2010 Capturing Tabular Data from Graphical Output Part 2: Web and Windows-Based Tools Brian P. Fairfield-Carter,
Stephen Hunt		 11
PharmaSUG 2010 Clinical Programming For Novice Ramesh Ayyappath 5
PharmaSUG 2010 SDD Unleashed - Extending the Capabilities of SAS Drug Development Stephen Baker 10
SGF 2010 Analytics in the Converging Health and Life Sciences Industries: The Catalyst for the Next Generation of Healthcare Matt Gross source 15
SGF 2010 Clinical Trials Simulation: A Publicly Available, Grid-Enabled, GUI-Driven SAS System Peter H. Westfall,
Alex Dmitrienko,
Cynthia DeSouza,
Alin Tomoiaga		 source 13
SGF 2010 Reverse-Engineer a Reference Curve: Capturing Tabular Data from Graphical Output Brian P. Fairfield-Carter source 6
SGF 2010 The Past, Present, and Future of Clinical Data Standards Chris Decker source 10
SESUG 2009 Importing Complicated Excel Files into SAS Drug Development (SDD) Heather L. Murphy,
Gregory C. Steffens		 source 11
PHUSE EU 2009 A Framework for Acheiving an Industry-Driven, Open-Source Clinical Reporting System Dante Di Tommaso,
Ann Marie Martin		 source 5
PHUSE EU 2009 Acceleration through Collaboration Carrie Eason source
presentation source		 7
PHUSE EU 2009 An Application of SAS in Model Based Drug Development Imelda Parker,
Michael O'Kelly		 source 4
PHUSE EU 2009 Automation using SAS & C#.NET for CROs and Pharmaceuticals Giri Balasubramanina,
Gopinath Viswanathan		 source
presentation source		 13
PHUSE EU 2009 Challenges in running a virtual department through outsourcing Silvana Cappi source 7
PHUSE EU 2009 Kendle Implementation of CDASH [presentation] Elke Sennewald,
Gill Lawrence		 source 32
PHUSE EU 2009 Lean/Six Sigma..the 5 why's [presentation] Michael Whitworth source 32
PHUSE EU 2009 Medical Data Review in Exploratory Drug Development Michaela Jahn,
Joshua Haznedar		 source
presentation source		 21
PHUSE EU 2009 Medical Research: What should Programmers prepare for? Emilie Brennion source 12
PHUSE EU 2009 ModSpace: Promoting Modeling Dissemination and Reuse Jonathan Chard,
Henning Schmidt		 source
presentation source		 9
PHUSE EU 2009 The Pharmaceutical Industry is under pressure to evolve for many reasons. How does this impact on the role of the Statistician and Statistical Programmers? Gail Kniveton source 15
NESUG 2009 Sol LeWitt and the CDISC Initiative: A Comparative Essay Karin LaPann 10
NESUG 2009 Supporting CDISC Standards in Base SAS Using the SAS Clinical Standards Toolkit Peter Villiers 13
WUSS 2009 BRIDGing CDASH to SAS: How Harmonizing Clinical Trial and Healthcare Standards May Impact SAS Users Clinton Brownley source 6
PharmaSUG 2009 A Framework For Achieving An Industry-Driven, Open-Source Clinical Reporting System Dante Di Tommaso,
Ann Marie Martin,
Paul OldenKamp,
Paul D. Hamilton		 6
PharmaSUG 2009 Biostatistics and Data Management - A match made in ... Tasmania? Elaine Dempsey 2
PharmaSUG 2009 Implementation Plan for CDISC SDTM & ADaM Standards at MedImmune Alan Meier 11
PharmaSUG 2009 Medical Coding System for Clinical Trials - 21 CFR Part 11 Compliant SAS/AF Application Annie S. Guo 12
PharmaSUG 2009 Supporting CDISC Standards in Base SAS Using the SAS Clinical Standards Toolkit Supporting CDISC Standards 13
SGF 2009 Clinical SAS Programming: Analysis and Mitigation of Risk Parag Shiralkar source 6
SGF 2009 Retirement of Legacy Clinical Systems and Moving to SAS Drug Development, Much More than Just Moving the Data Fred R. Forst,
John Standefer		 source 17
SGF 2009 Supporting CDISC Standards in Base SAS Using the SAS Clinical Standards Toolkit Peter Villiers source 13
SGF 2009 Talking Past Each Other? How to Communicate with Medical Writers When Preparing Clinical Research Manuscripts for Journal Submission Scott C. Thompson,
Stephanie R. Thompson		 source 7
SESUG 2008 Building a Clinical SAS Programming Group from the Ground Up Devin J. Hunt source 4
PHUSE EU 2008 Biostatistics and Data Management - A match made in ... Tasmania? Elaine Dempsey source 2
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 Decimaker: A statistical software using R, Microsoft .NET, R (D)COM Server and graphical libraries Julien Vanwinsberghe,
Francois Vandenhende		 source 10
PHUSE EU 2008 Developing a clinical reporting system collaboratively under an Open Source software license. Ann Marie Martin source 7
PHUSE EU 2008 Using SAS 9 in Clinical Research Gregory S. Barnes Nelson source 11
NESUG 2008 Talking Past Each Other? How to Communicate with Medical Writers When Preparing Clinical Research Manuscripts for Journal Submission Scott C. Thompson,
Stephanie R. Thompson		 7
PharmaSUG 2008 Case Report Form Auto-Annotation in PDF Files with a Metadata Database and SAS ODS XML Tagsets in a Data Management Unit David M. Escobar,
Ann Fowler,
Barbara Mathewson		 5
PharmaSUG 2008 SAS, CDISC and Clinical Data Integration Peter Villiers 27
PharmaSUG 2008 The CDISC Study Data Tabulation Model (SDTM): History, Perspective, and Basics Fred Wood 8
PharmaSUG 2008 Validating CDISC SDTM-Compliant Submission-Ready Clinical Datasets with an In-House SAS Macro-Based Solution Bhavin Busa,
Sheila Vince,
Jameelah Aziz		 12
SGF 2008 The Evolution of SAS in Life Sciences Research and Development David Handelsman source 10
SGF 2008 Using Regression Diagnostics and Clustering Criteria to Uncover ID Errors David J. Pasta,
Eric P. Elkin,
Rory Michaelis		 source 10
SGF 2008 Using SAS as an Integrated Component of the Clinical Research Information System Christopher W. Schacherer,
Jeffrey E. Gershenwald		 source 11
WUSS 2007 Using Regression Diagnostics and Clustering Criteria to Uncover ID Errors David J. Pasta,
Eric P. Elkin,
Rory Michaelis		 source 10
PHUSE EU 2007 A dedicated programming group in a pharma M&S organization Vincent Buchheit source 8
PHUSE EU 2007 Bayesian Modelling with SPLUS and the S+flex Bayes library Andrew Jack,
Dawn Woodard		 source 11
PHUSE EU 2007 Clinical Research Information Management... David Handelsman source 8
PHUSE EU 2007 Data mining in the clinical research environment David Smith source 7
PHUSE EU 2007 Designing a Global SAS9 Architecture for analysis and reporting Andrew York,
Gregory S. Barnes Nelson		 source 26
PHUSE EU 2007 Integrating data transformations using DI Studio and SAS DD Alistair Dootson source 15
PHUSE EU 2007 LSLV to Final CSR Tables in 24 hours - Dream or Reality? Stinder Fowler source 10
PHUSE EU 2007 The perfect reporting system - theoretically Laura Phelan,
Magnus Mengelbier		 source 7
PHUSE EU 2007 WEB-TRIAGE: Application for patient registration in ph I studies Angelo Tinazzi,
Lucio Ferraresi		 source 10
PharmaSUG 2007 Designing and Building an Administrative Model for SAS Drug Development Margaret M. Coughlin 6
PharmaSUG 2007 PROC REPORT or DATA _NULL_: Which to Use and How to Make it Easier David W. Carr 11
PharmaSUG 2007 The Use of CDISC Standards in SAS from Data Capture to Reporting Andrew T. Fagan 21
PharmaSUG 2007 Using SAS 9 in Clinical Research Gregory S. Barnes Nelson 11
SGF 2007 ODS Statistical Graphics for Clinical Research Wei Cheng source 20
PHUSE EU 2006 Contours of a Drug Development Data Warehouse Paul Vervuren source 8
PHUSE EU 2006 Integrating Specialized Graphics and Analysis into Production Systems Joel M. Hoffman,
Michael O'Connell		 source 18
PHUSE EU 2006 Interfering with Data Management by the Statistician Jim Groeneveld source 6
PHUSE EU 2006 Statistical Graphics and Reporting in Drug Development Michael O'Connell,
Sven Knudsen		 source 13
PHUSE EU 2006 Statistics and Pharmacokinetics in Clinical Pharmacology Studies Amy Newlands source 8
PHUSE EU 2006 The Hazards of Modelling Proportional Hazards in SAS Erika Daly,
Farzana Sufi		 source 4
PHUSE EU 2006 The Power of RETAIN Statement in Clinical Trial Programming by Examples Baoxian Lan source 5
PHUSE EU 2006 The Use of CDISC Standards in SAS from Data Capture to Reporting Andrew T. Fagan source 21
PHUSE EU 2006 Titles and Footnotes Macro Jennie McGuirk,
John Woods		 source 8
NESUG 2006 Designing and Building an Administrative Model for the SAS Drug Development Tool Meg Coughlin 6
PharmaSUG 2006 De-Identification of Clinical Trials Data Demystified Jack Shostak 12
PharmaSUG 2006 SAS Drug Development: Bringing Innovation to Life Sciences David Handelsman 12
SUGI 2006 Empirical Power Estimation for Phase I Dose-Proportionality Studies Based on Power-Law Model Using Confidence Interval Criteria Jihao Zhou,
Jane Li,
Bruce Coate,
Melissa Chen		 source 11
SUGI 2006 ODS Statistical Graphics for Clinical Research Wei Cheng source 10
PHUSE EU 2005 An Introduction to CDISC - CDISC Collaborations and Standards in Progress Becky Kush source 46
PHUSE EU 2005 An Introduction to CDISC - What is CDISC and Why Standards? Laurie Rose,
Becky Kush		 source 41
PHUSE EU 2005 Best Practices for Managing Clinical Research Information David Handelsman source 16
PHUSE EU 2005 CDISC Activities in Europe Udo Siegmann source 15
PHUSE EU 2005 How can you make the entire clinical trial process easy and fun for the users and also reduce your costs? Carl-Olow Magnusson,
Ann-Sofie Bergstrom		 source 1
PHUSE EU 2005 Technical application of SAS ETL Studio in the clinical reporting process David Smith source 8
PHUSE EU 2005 The Future of CDISC Becky Kush source 50
PHUSE EU 2005 Visions of a Drug Development Data Warehouse Paul Vervuren source 7
PHUSE EU 2005 What SAS is doing for the FDA's Critical Path Initiative? Andrew T. Fagan source 20
WUSS 2005 A Regulatory Compliant Process for Developing SAS-Based Reports Chuck Reap source 15
WUSS 2005 ODS Statistical Graphics for Clinical Research Wei Cheng source 20
PharmaSUG 2005 Get Experience with New SAS Drug Development Software Dana Rafiee 5
PharmaSUG 2005 Implementation of the CDISC SDTM at the Duke Clinical Research Institute Jack Shostak 12
PharmaSUG 2005 Proc Telecommute Susan Bairnsfather,
Angela S. Ringelberg		 5
SUGI 2005 A Regulatory Compliant Process for Developing SAS-Based Reports Chuck Reap source 15
NESUG 2004 Using SAS Drug Development as a Report Management Application Barry R. Cohen 8
NESUG 2004 Web Services Integration and the SAS Drug Development Platform Christopher R. Olinger,
John Leveille		 14
SCSUG 2004 SAS Enterprise Guide 3.0 for SAS Programmers - A Roadmap to Combining the Best of Both Worlds Stephen McDaniel,
Annette McDaniel,
Gregory A. Smith		 3
MWSUG 2004 SAS Enterprise Guide 3.0 for SAS Programmers - A Roadmap to Combining the Best of Both Worlds Stephen McDaniel,
Annette McDaniel,
Gregory A. Smith		 3
PharmaSUG 2004 Using SAS Drug Development as a Report Management Application Barry R. Cohen 8
PharmaSUG 2004 Web Services Integration and the SAS Drug Development Platform Christopher R. Olinger 14
SUGI 2004 Data Management in Analyzing Clinic Trial Data - Metadata Application Julia Z. Zhang,
David C. Chen		 source 6
SUGI 2004 SAS Enterprise Guide 3.0 for SAS Programmers - A Roadmap to Combining the Best of Both Worlds Stephen McDaniel source 4
NESUG 2003 Audit Trails of SAS Data Set Changes -- An Overview Maria Y. Reiss 9
NESUG 2003 Using SAS Drug Development as a Report Management Application Barry R. Cohen 8
SEUGI 2003 An Introduction to Genomics and SAS Scientific Discovery Solutions [presentation] Karen Miller source 34
SEUGI 2003 OPIS - A Web Enabled Clinical Data Warehouse Prototype [presentation] Claus Puhr source 24
SEUGI 2003 The Value of Text Mining in Pharmaceutical Laboratories [presentation] Elisabeth Maurice source 29
PharmaSUG 2003 Progress Toward Standardization of Submissions with the Electronic Common Technical Document and the Evolving Standardization of Clinical Data Susan Bairnsfather 8
PharmaSUG 2003 Standardizing Data Processing and e-Publishing for the Pharmaceutical Industry Shawn Wang 6
PharmaSUG 2003 Using SAS Drug Development as a Report Management Application Barry R. Cohen 8
SUGI 2003 Metadata Application on Clinical Trial Data in Drug Development Julia Z. Zhang,
David C. Chen,
Tor-lai Wong		 source 3
NESUG 2002 Using SAS Indexes with Large Databases Alexander Vinokurov,
Larry Helbers		 4
SEUGI 2002 A data warehouse and data exploitation solution in clinical trials [presentation] F. Patarnello,
V. Frizzo		 source 24
SEUGI 2002 SAS and the CRO [presentation] Peter Stagg source 14
SEUGI 2002 SAS Drug Development: Intelligent Research Management [presentation] Andrew T. Fagan source 18
PharmaSUG 2002 Implementing a Standardized Data Model - A Real Life Experience Curtis Wolf,
Paul M. Gilbert		 4
PharmaSUG 2002 IND Annual Reporting at a Glance Kristi Wiser 6
SUGI 2002 Unit-of-Analysis Programming Vanessa C. Hayden source 6
NESUG 2001 SynCoder: A SAS/AF Application for Implementing MedDRA Coding in Clinical Trials Deborah A. Testa,
Russell Holmes,
Daphne Ewing		 3
SEUGI 2001 Web and Data Warehouse technology combined in a pharmaceutical decision support system [presentation] Christine Vander Vorst source 29
PharmaSUG 2001 FDA Reviewers as Ultimate End Users: Using the SAS System to Construct e-Submissions that Actually Facilitate the NDA / BLA Review Process Rich Vachal 6
PharmaSUG 2001 SynCoder: A SAS/AF Application for Implementing MedDRA Coding in Clinical Trials Deborah A. Testa,
Russell Holmes,
Daphne Ewing		 4
PharmaSUG 2001 Unit-of-Analysis Programming Vanessa C. Hayden,
Fidelity Investments		 6
SUGI 2001 Integrating SAS in Corporate IT John M. LaBore,
Thomas H. Burger		 source 6
SESUG 2000 Integrating SAS in Corporate IT John M. LaBore source 6
SESUG 2000 Positioning SAS Software for Corporate Effectiveness John M. LaBore source 6
NESUG 2000 SynCoder: A SAS/AF Application for Implementing MedDRA Coding in Clinical Trials Deborah A. Testa,
Russell Holmes,
Daphne Ewing		 3
MWSUG 2000 Positioning SAS for Corporate Effectiveness John M. LaBore,
Thomas H. Burger		 6
SEUGI 2000 Clinical Data Warehousing Functionality [presentation] Michael Roberson source 39
SEUGI 2000 Genetic Data Analysis with Enterprise Mineer [presentation] John C. Brocklebank,
Wayne Thompson		 source 24
SEUGI 2000 Intergrating SAS in Corporate IT John M. LaBore,
Thomas H. Burger		 source 6
SEUGI 2000 Positioning SAS Software for Corporate Effectiveness John M. LaBore,
Thomas H. Burger		 source 6
SEUGI 2000 Successful and Faster Drug Development through Data Mining [presentation] Dirk Belmans source 15
PharmaSUG 2000 Clinical Data Warehouse Functionality Peter Villiers 5
PharmaSUG 2000 Constructing a Data Warehouse for Pharmacokinetic Data Stanley P. Koprowski Jr.,
Jeffrey S. Barrett,
Dwight J. Fowler		 9
PharmaSUG 2000 Integrating SAS in Corporate IT John M. LaBore 6
PharmaSUG 2000 SynCoder: A SAS/AF Application for Implementing MedDRA Coding in Clinical Trials Deborah A. Testa,
Russell Holmes		 2
SUGI 2000 Constructing a Data Warehouse for Pharmacokinetic Data Stanley P. Koprowski Jr.,
Dwight J. Fowler,
Jeffrey S. Barrett		 source 7
SUGI 2000 Positioning SAS Software for Corporate Effectiveness John M. LaBore,
Thomas H. Burger		 source 6
SUGI 2000 SynCoder: A SAS/AF V7/8 Application for Implementing MedDRA Coding in Clinical Trials Deborah A. Testa,
Russell Holmes		 source 2
MWSUG 1999 Positioning SAS for Corporate Effectiveness John M. LaBore,
Thomas H. Burger		 6
SEUGI 1999 Overview of pharma technology process model components [presentation] Patrick O'Donoghue,
Tim Thompson		 source 40
SESUG 1998 Building Clinical Information Spaces on the World Wide Web Paul C. Wehr 4
SEUGI 1998 Electronic documentation of statistical workflow in clinical research using a SAS application [presentation] Merras Teo source 9
PharmaSUG 1998 Building Clinical Information Spaces on the World Wide Web Paul C. Wehr 4
SUGI 1998 Building Clinical Information Spaces on the World Wide Web Paul C. Wehr source 4
SUGI 1998 Using the Data Warehouse Model to Streamline and Accelerate New Drug and Medical Device Development Martin J. Rosenberg source 5
WUSS 1997 Using the Data Warehouse Model is Streamline and Accelerate New Drug and Medical Device Development Martin J. Rosenberg source 5
SEUGI 1997 Understanding and enforcing standards to promote efficiency Meimei Ma,
Sandra D. Schlotzhauer		 source 9
PharmaSUG 1997 ClinAccess: An Integrated Client/Server Approach to Clinical Data Management and Regulatory Approval Martin J. Rosenberg 9
PharmaSUG 1997 How To Create a Simple SAS/AF Interface For Existing Batch Applications Bryan K. Beverly 4
SUGI 1997 Issues Concerning Consultant-Client Interactions: Things I learned at the Information Center Ioannis C. Dimakos source 3
SUGI 1997 Manipulating Clinical Research Data with the TRANSPOSE Procedure in SAS/ASSIST Software Stanley Cron source 2
SESUG 1996 Mission Impossible: The Trials of SAS Support in a Health Care Research Group Miriam W. Rosenblatt 6
WUSS 1996 ClinAccess: An Integrated Client/Server Approach to Clinical Data Management and Regulatory Approval Martin J. Rosenberg source 9
WUSS 1996 Design, Analysis and Review Tools for Clinical Drug Development Using SAS Object-Oriented Products David H. Christiansen source 8
PNWSUG 1996 ClinAccess: An Integrated Client/Server Approach to Clinical Data Management and Regulatory Approval Martin J. Rosenberg 9
SEUGI 1996 Re-engineering the CAPLA: integrating electronic submissions into the drug development Guy Pawson source 34
SUGI 1996 ClinAccess: An Integrated Client/Server Approach to Clinical Data Management and Regulatory Approval Martin J. Rosenberg source 9
SUGI 1996 Mission Impossible: The Trials of SAS Support in a Health Care Research Group Miriam W. Rosenblatt source 6
SUGI 1996 Tips and Techniques for Data Fixes in a Repository Data Warehouse Ty Lee source 6
SUGI 1996 Using SAS Software to Perform Meta-Analytic Integrations Stanley G. Cran source 5
NESUG 1995 The Choice of SAS Software as the Application Development Tool for Your CANDA Barry R. Cohen 9
WUSS 1995 ClinAccess: An Integrated Client/Server Approach to Clinical Data Management and Regulatory Approval Martin J. Rosenberg source 9
WUSS 1995 Tips and Techniques for Data Fixes in a Repository Data Warehouse Ty Lee source 6
SEUGI 1995 Data Warehousing and CANDA Concepts for Biometry Ulrich Burger source 7
SUGI 1995 Click, Click, Click: Redesigning a Business Process Using FRAME Objects in SAS/ AF Software Deborah A. Testa,
Karen M. Michiels,
Thomas K. Lim		 source 4
SUGI 1995 ClinAccess: A Client/Server Approach to Clinical Trials Data Management and Regulatory Approval Martin J. Rosenberg source 7
SUGI 1995 The Intricate Organization and Management of Clinical Research Laboratory Samples Using SAS/AF Jacqueline A. Wendel,
Daniel Nosek		 source 6
NESUG 1994 Computer-Aided Software Engineering and SAS in Clinical Trials Reporting W. Stetson Line 6
NESUG 1994 Managing Clincial Lab Data with SAS/aF - an Outline Demonstration Eric C. Brinsfield,
Brad Klenz		 4
SEUGI 1994 A Unique Application Generator for the Management and Control of Clinical Trials Data Chaim Singal source 9
SEUGI 1994 Aiming at More Efficient System Support for the R&D Process Mark Crawford,
Winfried Koch		 source 8
SEUGI 1994 Budgeting Clinical Trials Using the SAS System Development Environment Patrick Genyn source 10
SUGI 1994 A Case Study in the Use of SAS/PH-Clinical for an Electronic Regulatory Submission of a Megatrial Kathy R. Boussina,
Dorene M. Emmrich,
Guy Pawson,
Alan Hopkins		 source 11
SUGI 1994 Developing Integrated Clinical Trials Systems: The ClinAccess Experience Martin J. Rosenberg source 7
SUGI 1994 Managing Clinical Lab Data with SAS/ AF Software - an Online Demonstration Eric C. Brinsfield,
Bradley W. Klenz		 source 4
WUSS 1993 An Integrated Clinical Trials System Utilizing Client Server and Graphical User Interface Technology Martin J. Rosenberg source 7
SEUGI 1993 A Generic Data Listing System Developed for Pharmaceutical Reporting Peter Fursdon source 11
SEUGI 1993 Integrated Safety Reporting Anemone Thalman source 10
SUGI 1993 An Integrated Clinical Trials System Utilizing Client Server and Graphical User Interface Technology Martin J. Rosenberg source 7
SUGI 1993 Re-engineering the Drug Development Process with 'the SAS Information Delivery System Bryan K. Beverly source 5
SUGI 1993 SAS/PH-Clinical Software: CANDA Implementation Strategies Juliana M. Ma,
Sandra D. Schlotzhauer		 source 8
SEUGI 1992 Improve Speed and Quality in Clinical Trial Analysis Using SAS Macros Mark de Somer source 12
SEUGI 1991 STARS: Statistical and Reporting System for Clinical Research Data A. Longoni,
G. Marcon,
M. Sanarico,
R. Ferrara		 source 7
SUGI 1991 A Clinical Data Review System to Facilitate Pharmaceutical Research Martin J. Rosenberg source 9
SUGI 1991 A Data Entry Application in Clinical Research Using Quality Assurance Tools Miriam W. Rosenblatt source 6
SUGI 1991 Using SAS Macro Language for Efficiency and Flexibility in Displaying Data for Clinical Trials Anne Brockley source 6
SUGI 1990 Shortcuts to Customize Clinical Trial Reports Aileen L. Tsien source 6
SUGI 1989 Determining the Roles of the SAS System and a Database Management System in Clinical Research Mark J. Holdbrook source 5
SUGI 1988 An Integrated Clinical Data Management System at Allergan, Inc. Jeffrey S. Kouba source 4
SUGI 1984 CPDMS-A Clinical Pharmacology Data Management System Rita Brilla,
Lorna Lyall,
Lois Preis		 source 7
SUGI 1982 SAS as a Convenient &Efficient Tool in the Management of Resources within an International Clinical Pharmacology Department A. E. Edelmann,
K.H. Jones,
M.A.P. Meisinger		 source 4
SUGI 1978 SAS as a Management System for Routine Echocardiograms Glenn A. Augustine,
Emilio R. Giuliani,
Kenneth P. Offord,
Vernon P. Weber		 source 2

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