Menu
×
Don't Miss Out!
Get your weekly Breakfast Briefing eNewsletter, filled with news, trends, and vital information from DIA!
DIA 2021 Global Annual Meeting
Advancing the Science of Patient Input: How are WE doing? Multi-Stakeholder Perspective
Session Chair(s)
Pujita Vaidya, MPH
- Director, Global Regulatory and R&D Policy, Patient Centricity, Pediatrics, ROD
- Amgen, United States
This forum will present current efforts and future opportunities to advance the incorporation of patient input into the medical product lifecycle. A panel of experts will discuss examples of how patient input have informed medical product decisions.
Learning Objective : Discuss current progress by key stakeholders in incorporating patient input into medical product development and regulatory decision-making; Discuss approaches and best practices to collect, analyze, assess quality, and present patient input; Identify opportunities for further enhancing the incorporation of patient input across the medical product lifecycle.
Speaker(s)
Panelist
Michelle Tarver, MD, PhD
- Deputy Director, Office of Strategic Partnerships & Technology Innovation, CDRH
- FDA, United States
Panelist
David S. Reasner, PhD
- Division Director, Division of Clinical Outcome Assessment, OND, CDER
- FDA, United States
Panelist
Annie Kennedy
- Chief of Policy, Advocacy, and Patient Engagement
- EveryLife Foundation for Rare Diseases, United States
Panelist
Jessica S. Scott, JD, MD
- President
- Legacy Health Strategies , United States
Panelist
Robyn T. Carson, MPH
- Vice President, Patient-Centered Outcomes Research
- AbbVie, United States