Colorado State University
Hilton Fort Collins
Fort Collins, Colorado
Author/Title
Abstract
Richard
K. Burdick Using
Tolerance Intervals for Setting Process Validation Acceptance Criteria
Christy
Chuang-Stein Statisticians
in the Pharmaceutical Industry: The 21st Century
Scott
Evans - Chair
Bob
O'Neill Karl Peace
Christy Chuang-Stein
Janet Wittes
Marvin Zelen The
Future of the Education of Clinical Trial Statisticians: What Changes
are Needed?
Dean
Follman Shared
Random Parameter Models for Informative Missing Data
Joseph
F. Heyse False
Discovery Rates for Discrete Data
Jason
C. Hsu Statistical
Principles for Design and Analysis of Pharmacogenomics Studies
Dallas
E. Johnson On
the Analysis of Crossover Designs
Karen Kafadar Statistics
and Biopharmaceutical Research: Bioinformatics, Massive Data, and
Computational Challenges
Craig Mallinckrodt An
Analytic Road Map for Incomplete Longitudinal Clinical Trial Data
Gert Molenberghs Every
Missing Not At Random Model Has Got a Missing At Random Counterpart with
Equal Fit
Robb
Muirhead Recent
Developments in the Analysis of QT Interval Data
Bob
O'Neill
Emerging Trends in Regulatory
Biostatistics - What Might be Their Impact ?
John
J. Peterson A
Bayesian Approach to the ICH Q8 Definition of Design Space
Katy
L. Simonsen Fun
with Genome Scans: Lessons in Multiplicity from Whole-Genome Association
Studies
Carrie
Green Wager Generalized
Equivalence Testing for Similarity
Sue-Jane
Wang Adaptive
Designs that Prospectively Learn versus Test Biomarker Sensitive
Patients
L.J.
Wei Model
Estimation, Checking and Evaluation via Prediction
Janet
Wittes Safety,
Can You Paradigm? A Statistical Lament
Graybill Conference
VII June 11-13, 2008
Colorado State University
Hilton Fort Collins
Fort Collins, CO 80526
