JSM 2012 Online Program
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Online Program HomeActivity Details
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530 | Wed, 8/1/2012, 12:30 PM - 1:50 PM | CC-Ballroom 20D | |
Biopharmaceutical Section P.M. Roundtable Discussion (fee event) — Roundtables PM Roundtable Discussion | |||
Biopharmaceutical Section | |||
Organizer(s): Estelle Russek-Cohen, FDA/CBER | |||
WL11: | Existing Practice and New Trends in Bioassay — Lev Sirota, FDA | ||
WL12: | Postmarket Surveillance Issues — Theodore Lystig, Medtronic | ||
WL13: | Evaluation of Sex Differences in Clinical Studies — Chul Ahn, FDA/CDRH | ||
WL14: | Design a Clinical Trial: Sequential Design or Fixed Sample Size Design? — Judy Li, FDA | ||
WL15: | Testing the Assumptions of Proportional Hazards — | ||
WL16: | Guidelines on Handling Missing Data in Clinical Trials: Present and Future — Xin Zhao, Janssen Al ; Jianing Di, Janssen Alzheimer Immunotherapy R&D, LLC |
2012 JSM Online Program Home
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