JSM 2012 Online Program
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Online Program HomeActivity Details
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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 |
2012 JSM Online Program Home
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