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TL18: Analytical studies in In Vitro Diagnostics
*Yuqun Abigail Luo, FDA\CBER Keywords: There are in vitro assays regulated by FDA but also in vitro lab assessments are a part of just about all clinical trials. The analytical properties of these assays are critical but pose interesting statistical challenges. This session will discuss the complexity of precision studies including estimating variability in multivariate assays and estimating limit of detection and issues of method comparisons.
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Key Dates
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November 1, 2012
Online submission opens for session, short course, roundtable luncheon discussion, and Town Hall proposals -
December 31, 2012
Online submission for a session, short course, and Town Hall proposals closes @ 11:59 pm EDT -
February 12, 2013
Organizing/Planning Meeting, Shady Grove, MD -
March 1, 2013
Roundtable submission closes @ 11:59 pm EDT -
April 30 - May 22, 2013
Invited Abstract Submission Open -
June 4, 2013
Online Registration Opens -
August 9 - August 23, 2013
Invited Abstract Editing -
August 23, 2013
Short Course materials due from Instructors -
August 26, 2013
Housing Deadline -
September 9, 2013
Cancellation Deadline and Registration Closes @ 11:59 pm EDT -
September 16 - September 18, 2013
Marriott Wardman Park, Washington, DC
