April 24, 2024
Best Practices for Engaging Patients and Using the Patient Perspective Over the Device Lifecycle
Post Market Track
Given the changing landscape of communication tools and access to information through various mechanisms and platforms, how do we best engage with one another to capture and reflect patient interests? They are our customers and at the heart of what we do. In this session, you’ll hear strategies for making sense of information for purposes of developing products, gathering product experience, improving products, and notifying patients of product risks. Join us as we hear from FDA, industry, and patient advocacy experts, and then engage them with your questions!
Sean Boyd, Director, Office of Regulatory Programs Office of Product Evaluation and Quality, Center for Devices and Radiological Health (CDRH), FDA
Jessica Zeller, VP Quality, Regulatory & Public Affairs Counsel, Edwards Lifesciences