Faculty, fellows, students and staff who are involved or are interested in the development of new device technologies, i.e. robotics, mobile medical applications, software, in vitro diagnostics, etc., as well as the development of new intended uses of marketed devices, are invited to participate in an upcoming town hall meeting Wednesday, March 27, from 3 to 4 p.m. in 202 Light Hall.
All interested VU investigators are encouraged to attend.
The agenda for this town hall meeting will include an overview of Vanderbiltís new IDE process for compliance with FDA device regulation and a panel of VUMC investigators who will share their experiences with IDEs and the device development process. The panel will be followed by a question and answer session. This is an excellent opportunity for the research community to engage in discussion regarding the IDE process. The Town Hall will be led by Barbara Gibson, MS, Regulatory Affairs Officer, HRPP.
For more information about this meeting, please contact Barbara Gibson in the Vanderbilt Human Research Protection Program at email@example.com, or 875-8965.