Device Development from A to D: Getting on the same page to improve efficiency
-To describe the process of general device development from design to post-market assessment -To better understand the clinical and engineering challenges with device development -To identify clinical, engineering and regulatory needs required for device development
The Greenberg Stent Summit 2018 will evaluate the process by which an idea transforms into a clinical product. From inception to clinical trial. What is the role of industry, regulatory agencies, and clinicians?
* Previous Stent Summit agendas focused on areas of the arterial system (e.g., abdominal, thoraco-abdominal, ascending and arch) and various lesion types (e.g., dissection, aneurysm, stenosis).
InterContinental Hotel Boston
510 Atlantic Avenue
Boston, MA 02210
The discounted hotel room rate of $279.00 plus tax per night is available through Monday, August 6th or once the block reaches capacity. Please mention the Greenberg Stent Summit when calling for a reservation.
U.S. Food and Drug Administration
Matthew Eagleton, MD
Massachusetts General Hospital
Matt Waninger, PhD
Robert Whirley, PhD
For additional information, please contact Jamie Belkin Events at
216.932.3448 or firstname.lastname@example.org.