PharmaSUG2010 - Paper CD06
How to build ADaM from SDTM: A real case study
JIAN HUA (DANIEL) HUANG, FOREST LABORATORIES, NJ
ABSTRACT:
Building analysis data based on the ADaM model is highly recommended since ADaM supports a high
transparency of derivation
SAS Global Forum 2011
Posters
Paper 385-2011
WHAT CDISC MEANS TO SAS PROGRAMMERS
Kevin Lee, Cytel, Inc., Chesterbrook, PA
ABSTRACT
The paper is intended for SAS programmers in the pharmaceutical industry who are interested in SAS programming
in a CDISC en
PhUSE 2014
Paper CD13
Looking for SDTM Migration Specialist
Angelo Tinazzi, Cytel Inc., Geneva, Switzerland
ABSTRACT
Despite CDISC became a widely accepted standard for electronic data submission with US-FDA soon no longer
accepting non-CDISC submission a
PharmaSUG 2013 - Paper IB06
Introduction to the CDISC Standards
Sandra Minjoe, Accenture Life Sciences, Wayne, Pennsylvania
ABSTRACT
The Clinical Data Interchange Standards Consortium (CDISC) encompasses a suite of standards across the clinical
space. The
SDTM Implementation - Best Practices
Pantaleo Nacci, Head Statistical Safety & Epidemiology/PV
Biometristi Italiani Associati (BIAS) Seminar:
CDISC, SDTM and ADaM: Moving from theory to practice
SAS Institute - Milano, 14 March 2014
Agenda
The story so fa
SAS Global Forum 2008
Pharma, Life Sciences and Healthcare
Paper 207-2008
Practical Methods for Creating
CDISC SDTM Domain Data Sets from Existing Data
Robert W. Graebner, Quintiles, Inc., Overland Park, KS
ABSTRACT
Creating CDISC SDTM domain data sets fr
CDISC SDTM/ADaM Pilot Project1
Project Report
Executive Summary
Background
CDISC is a non-profit, multidisciplinary consensus based standards development
organization founded over a decade ago that has established open, worldwide
biopharmaceutical data st
Upgrading to IBM Cognos 10
Marc deLorimier
Solution Architect
State, Local & Higher Ed
1
Agenda
Approaches to upgrading
Supported upgrade path to Cognos 10
The basic upgrade workflow
Failing to plan is planning to fail
Some high-level proven practices
