CDISC Standards for Clinical Trial Data
*Chris Holland, FDA Keywords: Members of industry and the FDA are increasingly encouraging the implementation of CDISC standards for clinical trial data. While some organizations have adapted completely to the use of such standards, others have decided to take a “wait and see” approach. Thoughts and experiences from both ends of the spectrum, including those from FDA, are invited to be shared at this roundtable so that participants can decide whether they have jumped in too early, or are jumping in too late.
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Key Dates
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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