Investigational Device Exemption (IDE) Workshop

This course will offer best practices when conducting trials using FDA approved and non-approved devices.

When May 22, 2013 from 09:00 AM to 12:00 PM (US/Eastern / UTC-400)
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The workshop will cover the IDE application process and the obligations of the sponsor-investigator once the IDE application is filed with the FDA. For more information and to register, please click here.

These workshops are a CTSA collaboration by the NC TraCS (Translational and Clinical Sciences) Institute and the Duke Translational Medical Institute (DTMI).

The IND and IDE Workshops have each been pre-approved for 3 Contact Hours of Clinical Research Education for re-certification of ACRP’s CCRC®, CCRA®, CPI®, at no cost. Certificates of attendance will be available at the conclusion of the training. For nurses or others in need of Continuing Education Units, 3 CEUs are available at a cost of $6 per day (please provide payment in the form of a check and your PID number on the day of training).