JSM 2011 Online Program
The views expressed here are those of the individual authors and not necessarily those of the JSM sponsors, their officers, or their staff.
Activity Details
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192 | Mon, 8/1/2011, 12:30 PM - 1:50 PM | CC-JR Ballroom D | |
Biopharmaceutical Section P.M. Roundtable Discussions (fee event) — Roundtables PM Roundtable Discussion | |||
Biopharmaceutical Section | |||
Organizer(s): Carmen Mak, Schering Plough Research Institute | |||
ML10: | Implementation and Logistics of Adaptive Trial Design — Eva R. Miller, ICON Clinical Research | ||
ML11: | Statistical Issues in the Design and Analysis of Dose-Response Studies — Susan Huyck, Merck Research Laboratories | ||
ML12: | Effect of Subsequent Therapies After Discontinuation of Study Medication in Analyzing Overall Survival in Cancer Clinical Trials — Julie Xiuyu Cong, Boehringer Ingelheim | ||
ML13: | Analysis of Longitudinal Categorical Data — Madhuja Mallick, Merck Research Laboratories | ||
ML14: | CANCELLED: Impact of the Noninferiority Clinical Trials Draft FDA Guidance on Noninferiority Margins Interpretation — Claude Petit, Boehringer Ingelheim | ||
ML15: | Health Care Reform, Baby Boomers, and the Pharmaceutical Industry — T. Paulette Ceesay, Merck & Co., Inc. ; Darcy Hille, Merck & Co., Inc. |
2011 JSM Online Program Home
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