Clinical Compliance 2012 - Best Practices for Maintaining an IND and IDE Application with FDA
Date2012-03-21
Deadline2012-03-21
VenuePalo Alto, USA - United States
KeywordsFDA IND Application; IDE Application; IND submission; IDE submission; Suspending IND reopening IND; IND closure, withdrawing an IND, IDE application management
Topics/Call fo Papers
This webinar on IND and IDE Application management will help you understand the current FDA requirements for IND and IDE application post initial approval to proceed with the clinical trial.
Why Should You Attend:
If your company has active IND or IDE applications with the FDA or are planning to file one soon, this seminar will help you understand the current FDA requirements for IND and IDE application post initial approval to proceed with the clinical trial.
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Last modified: 2012-02-16 14:32:49