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FDA/PhUSE CSS Conference Proceedings: FDA/PhUSE US Computational Science Symposium 2012
March 19-20, 2012, Silver Spring, Maryland, 21 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/posters]

FDA/PhUSE US Computational Science Symposium 2012: Best Papers and honorable mentions

Preparing Data for Submission to the FDA - It's More Than SDTM
  Bruce Thompson, C-TASC (Winning Poster in Posters)
An Evaluation of Data Mining Methods and Software for Adverse Events Occurring in Clinical Trials
  Paul Schuette, FDA (1st Runner Up in Posters)
Adaptive Trials and the Impact on STDM Trial Design Model
  Nate Freimark, Theorem Clinical Research (2nd Runner Up in Posters)

Posters

Posters
Winning Poster
tweet!  Preparing Data for Submission to the FDA - It's More Than SDTM
  Bruce Thompson, C-TASC
Keywords: scientific research template custom poster presentation symposium printing PowerPoint create design example sample download
Pages: 1 Size: 2088 Kb 
1st Runner Up
tweet!  An Evaluation of Data Mining Methods and Software for Adverse Events Occurring in Clinical Trials
  Paul Schuette, FDA
Pages: 1 Size: 431 Kb 
2nd Runner Up
tweet!  Adaptive Trials and the Impact on STDM Trial Design Model
  Nate Freimark, Theorem Clinical Research
Pages: 1 Size: 322 Kb 
tweet!  Path to Metadata-Driven Standards Environment - Collection to Submission
  Melissa Binz, Novartis Pharmaceuticals Corporation
Pages: 1 Size: 4919 Kb 
tweet!  SAS Template Programs for Building Derived Datasets, Tables and Listings
  Michael Carniello, Takeda Global R&D
Pages: 1 Size: 324 Kb 
tweet!  Automatic Version Control and Track Changes of CDISC ADaM Specifications for FDA Submission
  Min Chen, Vertex Pharmaceuticals
Pages: 1 Size: 158 Kb 
tweet!  Risk Based SDV (Source Data Verification)
  Shafi Chowdhury, Shafi Consultancy
Pages: 2 Size: 2626 Kb 
tweet!  An Innovative ADaM Programming Tool for FDA Submission
  Xiangchen (Bob) Cui
Pages: 1 Size: 176 Kb 
tweet!  Achieving an 'Error Free' OpenCDISC Report - Realistic or Idealistic?
  Ratnakar Gundlapalli, ICON Plc
Pages: 1 Size: 370 Kb 
tweet!  Throwing Data Over the Wall: The Next Big Threat to Clinical Data Quality
  Kit Howard, Kestrel Consultants Inc
Pages: 1 Size: 1103 Kb 
tweet!  The Clinical Data Repository Initiative at Novartis Vaccines and Diagnostics: A Revolution
  Pantaleo Nacci, Novartis Vaccines and Diagnostics
Pages: 1 Size: 847 Kb 
tweet!  Nonclinical Safety Data Integration Platform
  Alain Nanzer, F.Hoffman-La Roche Ltd
Pages: 1 Size: 714 Kb 
tweet!  Standardization in Medical Research Data: Improving Data Displays and Data Traceability
  Mary Nilsson, Eli Lilly & Company
Pages: 1 Size: 1535 Kb 
tweet!  Describing Data from Capture to Operational Use to CDISC-Compliant Submission
  Yun Oldshue, Takeda Global R&D
Pages: 1 Size: 3158 Kb 
tweet!  Using SAS® to Calculate Noncompartmental Urine Parameters
  Vanessa Rubano, Boehringer Ingelheim Pharmaceuticals USA
Pages: 1 Size: 141 Kb 
tweet!  Automation of Clinical Trial Reporting: From Shells to TFL Outputs Without a Single Line of SAS Code
  Francois Vandenhende, Clinbay
Pages: 1 Size: 1407 Kb 
tweet!  Comparing the Risk-Benefit of SDTM Software Solutions
  Michael Wall, Pharstar
Pages: 1 Size: 375 Kb 
tweet!  Optimizing the Organizational Performance of the Clinical Trials Process Through Better Technology
  Michael Whitworth, Quanticate
Pages: 2 Size: 626 Kb 
tweet!  CDISC Standards in Reverse: A More Efficient Approach to Clinical Trials Design
  Robert Woolson, Rho Inc
Pages: 1 Size: 894 Kb 
tweet!  Business Process Management (BPM) at the FDA: The Agency's Early Experience in Implementing BPM SW Tools
  Markus Yap, FDA
Pages: 1 Size: 993 Kb 
tweet!  CDISC-AdvaMed Device Project
  Fred Wood, Octagon Research Solutions
Pages: 1 Size: 10168 Kb 
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