JSM Preliminary Online Program
This is the preliminary program for the 2006 Joint Statistical Meetings in Seattle, Washington.

The views expressed here are those of the individual authors
and not necessarily those of the ASA or its board, officers, or staff.


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Legend: = Applied Session, = Theme Session, = Presenter, Sheraton Seattle Hotel & Towers = “S”
Washington State Convention & Trade Center = “CC”, Grand Hyatt Seattle = “H”

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CE_28C Tue, 8/8/06, 8:30 AM - 5:00 PM CC-304
Bioequivalence and Statistics in Clinical Pharmacology - Continuing Education - Course
The ASA
Instructor(s): Scott Patterson, GlaxoSmithKline, Byron Jones, Pfizer Inc.
This course will cover the application and basic elements of the theory of statistical methods in clinical pharmacology. The morning will deal with techniques used in the assessment of bioequivalence---the study of a drug formulation to confirm its equivalence to another. The afternoon will focus on the use of statistics in clinical pharmacology studies of safety, ECG monitoring, efficacy, and population pharmacokinetics. The emphasis will be on study design, analysis, and interpretation of data using real-data examples from the authors' experiences. RECOMMENDED TEXTBOOK: Patterson, S. and Jones, B. (2005): Bioequivalence and Statistics in Clinical Pharmacology. CRC Press. ISBN: 1584885300.

Course attendees are expected to be familiar with the topic at the level of:
Design and Analysis of Cross-over Trials by B. Jones and M. Kenward, Chapman and Hall OR
Cross-over Trials in Clinical Research by Sean Senn, John Wiley and Sons.

 

JSM 2006 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.
Revised April, 2006