Home
Contact
SAS Paper Search
SAS:MWSUG papers
SAS:NESUG papers
SAS:PharmaSUG papers
SAS:PharmaSUG China papers
SAS:PhUSE papers
FDA/PhUSE CSS posters
SAS:PNWSUG papers
SAS:SCSUG papers
SAS:SESUG papers
SAS:SeUGI papers
SAS:SUGI papers
SAS:VIEWS papers
SAS:WUSS papers
SAS:CDISC papers
Fortune records
Marsh 1001
India
South America

Powered by SAS® 9.01.01M3P02162005.

Valid XHTML 1.0 Transitional

Google
  Search results
FDA/PhUSE CSS Conference Proceedings: FDA/PhUSE US Computational Science Symposium 2016
March 13-15, 2016, Silver Spring, Maryland, 30 papers
FDA/PhUSE CSS 2012   FDA/PhUSE CSS 2013   FDA/PhUSE CSS 2014   FDA/PhUSE CSS 2015   FDA/PhUSE CSS 2016   FDA/PhUSE CSS 2017  

[Original source: http://www.phuse.eu/css-presentations-2016]

FDA/PhUSE US Computational Science Symposium 2016: Best Papers and honorable mentions

PhUSE De-identification Working Group: Providing De-identification Standards to CDISC Data Models
  Jean-Marc Ferran, Qualiance; Kelly Mewes, Roche (Winning Poster in Posters)
The Nonclinical SDRG
  Gitte Frausing, Data Standards Decisions; Catherine Roy, Merck (Winning Poster in Posters)
Standard Endpoints, Standardized Data and Subgroup Outcomes in Diabetes: A Patient-Level Meta-analysis
  Crystal Allard, FDA; Tejaskumar Patel, FDA; Helena Sviglin, FDA (Winning Poster in Posters)

Posters

tweet!  You are the Concierge – a CDISC compliant project management tool on SDD
  Chen Shi, Santen Inc.
Keywords: poster presentation poster design poster template
Pages: 1 Size: 389 Kb 
Posters
tweet!  Using CDISC Standards and Semantic Technology to Drive the Automation of Study Database Build
  Chris Price, Roche; Jonthan Chainey, Genentech
Pages: 1 Size: 915 Kb 
tweet!  Proposal for Streamlining the SDRG and ADRG Authoring Process
  Stanely Wei, Novartis
Pages: 1 Size: 3021 Kb 
tweet!  Tough Start? Don't Panic! Your Submission Can Still Be Successful: Regulatory eSubmission Lessons Learned for a Late-stage Acquisition
  Jiaan Illidge, Alexion Pharmaceuticals; Chris Williams, Alexion Pharmaceuticals
Pages: 1 Size: 133 Kb 
NoSQL Database in Healthcare Industry
  Kevin Lee, Consultant
tweet!  Graphical Display of Histopathology Data from Toxicology Studies: An Industry Survey
  Alan Brown, Novartis; Philip Drew, PDS Consultants
Pages: 1 Size: 3204 Kb 
tweet!  Common Errors in Loading SDTM Data to the Clinical Trials Repository - Why Getting it Right Matters
  Crystal Allard, FDA; John Slattery, FDA
Pages: 1 Size: 402 Kb 
tweet!  Open-NCA - R Scripts for CDISC-based Pharmacokinetics Analysis
  Peter Schaefer, Validated Cloud Applications
Pages: 1 Size: 1305 Kb 
Winning Poster
tweet!  PhUSE De-identification Working Group: Providing De-identification Standards to CDISC Data Models
  Jean-Marc Ferran, Qualiance; Kelly Mewes, Roche
Pages: 1 Size: 2286 Kb 
tweet!  The Car is in the Shop but Where are the Mechanics? The Future of Standard Scripts for Analysis and Reporting
  Dirk Spruck, Clinipace Worldwide; Hanming Tu, Accenture; Dante Di Tommaso, Roche
Pages: 1 Size: 2711 Kb 
tweet!  Achieving Clarity through Proper Study Documentation: An Introduction to the Study Data Reviewer's Guide
  Terek Peterson, Chiltern; Michael Stackhouse, Chiltern
Pages: 1 Size: 775 Kb 
tweet!  Implementing NONMEM POP PK Specifications and Data Standards through the use of a Browser-based Form
  Robert Fox, AstraZeneca; Huan Liu, AstraZeneca
Pages: 1 Size: 412 Kb 
tweet!  Let's Visit "The Visits" Scheduled/Unscheduled: Windowing and Clinical Encounters
  Himajarani Surapaneni, Chiltern; Rama Devi Kudaravalli, Chiltern
Pages: 1 Size: 206 Kb 
tweet!  CDISC Standards End-to-End Transitional Hurdles
  Alyssa Wittle, Chiltern; Christine McNichol, Chiltern; Antony Cardozo, Chiltern
Pages: 1 Size: 147 Kb 
Winning Poster
tweet!  The Nonclinical SDRG
  Gitte Frausing, Data Standards Decisions; Catherine Roy, Merck
Pages: 1 Size: 528 Kb 
tweet!  Standard Analyses and Displays for Common Data in Clinical Trials - Socialize the Deliverables!
  Mary Nilsson, Eli Lilly; Nhi Beasley, FDA
Pages: 1 Size: 2017 Kb 
tweet!  Making 21 CRF a Linkable Resource for Semantic Web Applications
  Yu Lin, Rashedul Hasan; Mitra Rocca, FDA
Pages: 1 Size: 1227 Kb 
tweet!  Enhanced Visualization of Treatment Emergent Liver Effects in Integrated eDSH & Baseline Shift Plot
  Crystal Allard, FDA; Tejaskumar Patel, FDA, Nicholas Fleischer, FDA
Pages: 1 Size: 2940 Kb 
Winning Poster
tweet!  Standard Endpoints, Standardized Data and Subgroup Outcomes in Diabetes: A Patient-Level Meta-analysis
  Crystal Allard, FDA; Tejaskumar Patel, FDA; Helena Sviglin, FDA
Pages: 1 Size: 876 Kb 
tweet!  Common Data Quality Issues Identified During the JumpStart Process
  Crystal Allard, FDA; Kathryn Matto, IBM
Pages: 1 Size: 262 Kb 
tweet!  Screen-failure Data Provides Insight into Subgroup Representation in Diabetes Clinical Trials
  Crystal Allard, FDA; Tejaskumar Patel, FDA; Ana Szarfman, FDA
Pages: 1 Size: 692 Kb 
tweet!  Challenges in Legacy Data Mapping to SDTM Exposure Domains for Topical Drug Studies
  Aijun (Lillian) Qui, FDA; Hon-Sum Ko, FDA
Pages: 1 Size: 565 Kb 
tweet!  Collaboration with Safety Scientists Using Interactive Data Displays
  Xiangyun Wang, Genentech; Josephine Fong, Genentech
Pages: 1 Size: 378 Kb 
tweet!  Good Programming Practices at Every Level
  Maria Dalton, GSK
Pages: 1 Size: 170 Kb 
tweet!  Investigating Endpoint Modeling for SEND Datasets
  Christy Kubin, MPI Research; Brian Argo, MPI Research
Pages: 1 Size: 285 Kb 
tweet!  FDA SEND Submissions: Does the Pinnacle 21 Open-source Community Validator Predict FDA Findings?
  Laura Kaufman, PDS Life Sciences; Mike Wasko, PDS Life Sciences
Pages: 1 Size: 4616 Kb 
tweet!  Using Ebola Experiences to Highlight Standards Implementation in Outbreak Settings and Observational Studies
  Maura Kush, PharmaStat
Pages: 1 Size: 284 Kb 
tweet!  Statistical Computing Environments in the FDA's Center for Drug Evaluation and Research
  Paul Schuette, FDA
Pages: 1 Size: 142 Kb 
tweet!  Piloting Post-market Surveillance of Saxagliptin with FDA Adverse Event Reporting System and MedDRA-based Adverse Event Diagnostics
  Daniel Choi, FDA; Austin Taylor, FDA
Pages: 1 Size: 1354 Kb 
tweet!  The SEND Implementation Wiki- Crowd-sourced Practical SEND Information
  Christy Kubin, MPI Research; Lynda Sands, Independent Consultant
Pages: 1 Size: 1388 Kb 
Powered by SAS®.
SAS® and all other SAS Institute Inc. product or service names are registered trademarks or trademarks of SAS Institute Inc. in the USA and other countries.
Copyright © 1999-2017 Lex Jansen. All rights reserved.