Greenberg Stent Summit XIIIRegister Now
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).
U.S. Food and Drug Administration
Matthew Eagleton, MD
Massachusetts General Hospital
Matt Waninger, PhD
Robert Whirley, PhD
InterContinental Hotel Boston
510 Atlantic Avenue
Boston, MA 02210
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Harvard Club Downtown – Monday, August 27
Red Sox Game – Tuesday, August 28
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