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Activity Details

501 * Wed, 8/6/2014, 10:30 AM - 12:20 PM CC-251
Methods for Safety, Quality, and Benefit-Risk — Contributed Papers
Biopharmaceutical Section
Chair(s): T. Ceesay, Merck   
10:35 AM Mining Association Rules in Clinical Trial Safety Data Li Zhu, Amgen ; Amy Xia, Amgen ; Qi Jiang, Amgen ; Liron Walsh, Amgen ; William Go, Amgen
10:50 AM Revisiting Risks Ratio and Properties of Corresponding Confidence Intervals Ramin Arani, AstraZeneca ; Ian Hirsch, AstraZeneca
11:05 AM Multi-Criteria Decision Analysis for Benefit-Risk Analysis and Pharmaceutical Pricing Kao-Tai Tsai ; Bruce Dornseif, Celgene Corporation
11:20 AM Modeling Censored Stability Data Using Tobit Mixed Models Seth Clark, Merck
11:35 AM Using a Tolerance Region Approach as a Statistical Quality Control Process for Traditional Chinese Medicine Chinfu Hsiao, National Health Research Institutes ; Yi-Hsuan Lai, National Health Research Institutes
11:50 AM A Dynamic Bayesian Network Predictive Model with Stochastic Serial Structures in Detecting Safety Signals for Hematologic Responses in Cancer Patients Jagannath Ghosh, Novartis ; D. Das Purkayastha, Novartis
12:05 PM An Exposition to Integrated Modeling of Patients' Random Early Safety Signals for Effective Detections (Impressed): Cytogenetic, Molecular, and Hematologic Disorders — Sandip Acharya, Novartis ; D. Das Purkayastha, Novartis

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