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JSM 2012 Online Program

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Activity Details

118 * Mon, 7/30/2012, 8:30 AM - 10:20 AM HQ-Sapphire A
Modeling Issues in Clinical Trials of Medical Devices — Topic Contributed Papers
Biopharmaceutical Section
Organizer(s): John Evans, Boston Scientific Corporation
Chair(s): John Evans, Boston Scientific Corporation
8:35 AM Random Effect Multi-Stage Transitional Models Changhong Song, FDA/CDRH
8:55 AM Balance Diagnostics for Baseline Covariates in Nonrandomized Studies Involving Propensity Score Nelson Lu, FDA ; Weihua Cao, FDA ; Rajesh Nair, FDA
9:15 AM Reverse Regression in Randomized Clinical Trials with Nonignorable Nonresponse Zhiwei Zhang, FDA/CDRH ; Kyeongmi Cheon, National Institute of Child Health and Human Development
9:35 AM Impact of Various Modeling Options for Using GEE to Analyze Over-Dispersed Longitudinal Count Data Scott Miller, FDA
9:55 AM Limit of Blank, Limit of Detection, and Limit of Quantitation (Latest Changes in CLSI EP-17) Patrick Meyers, Abbott Laboratories
10:15 AM Floor Discussion

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