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This is the preliminary program for the 2009 Joint Statistical
Meetings in Washington, DC.
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The views expressed here are those of the individual authors and not necessarily those of the ASA or its board, officers, or staff. Back to main JSM 2009 Program page |
= Applied Session,
= Theme Session,
= Presenter
103
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Mon, 8/3/09, 8:30 AM - 10:20 AM | CC-149A |
| Postmarket Issues in Medical Devices - Topic Contributed - Papers | ||
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Biopharmaceutical Section |
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| Organizer(s): Vandana Mukhi, FDA | ||
| Chair(s): Vandana Mukhi, FDA | ||
| 8:35 AM |
Reporting of a Standardized Incidence Rate for Recurrent Adverse Events —  John C. Evans, Boston Scientific Corporation; Wen Ding, Boston Scientific Corporation; Jian Huang, Boston Scientific Corporation; Vivek Pradhan, Boston Scientific Corporation
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| 8:55 AM |
Statistical Practice and Post-Market Trials/Databases: Some Perspectives — Gosford A. Sawyerr, Purdue Pharma, LP
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| 9:15 AM |
Performance Characteristic of a Confidence Interval Approach for Safety Data Monitoring — Huyuan Yang, Boston Scientific Corporation; Haiying Lin, Boston Scientific Corporation; Hiroshi Fujimoto, Boston Scientific Japan K.K
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| 9:35 AM |
Can We Combine Multiple Condition of Approval Studies? — Shelby Li, Medtronic, Inc.; An Liu, Medtronic, Inc.; Hongyan Qiao, Medtronic, Inc.; Scott McRae, Medtronic, Inc.
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| 9:55 AM | Disc: Ning Li, FDA | |
| 10:15 AM | Floor Discussion | |
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JSM 2009
For information, contact jsm@amstat.org
or phone (888) 231-3473. If you have questions about the Continuing Education program,
please contact the Education Department. |