- February 3, 2020
9:30 AM - 11:30 AM ET
Understanding How the Public Perceives and Values Pharmaceutical Quality
February 3, 2020
Date: Monday, February 3, 2020
Time: 9:30 a.m. to 11:30 a.m.
Location: National Press Club, 529 14th St NW, Washington, DC 20045
Ensuring the quality of pharmaceutical products is essential and is part of the mission of the U.S. Food and Drug Administration (FDA). When pharmaceutical products do not meet quality standards, patients can be harmed or drug shortages can arise. Stakeholders, including patients, providers, pharmacists, drug purchasers, and payers, may each consider quality when making decisions about pharmaceuticals; however, very little research explores the role of quality in stakeholder decision-making.
This half-day public meeting, convened under a cooperative agreement between the Robert J. Margolis, MD, Center for Health Policy at Duke University in partnership with the FDA, will provide an opportunity to explore and better understand how stakeholders perceive and value the quality of pharmaceutical products. Key FDA leadership and staff will provide comments on the Agency’s current thinking and there will be opportunities for attendees to ask questions and engage with panelists. Topics for discussion include:
- The importance of pharmaceutical quality;
- The current state of pharmaceutical quality;
- FDA’s role in regulating quality; and,
- Stakeholder perceptions of pharmaceutical quality.
For a draft agenda, presentation slides, and a recording of the meeting please visit the Duke's Margolis Center for Health Policy website.
Register: In person attendance is limited, so please register at your earliest convenience. This event will also be webcast.
For further information, contact: Duke-Margolis Events, Duke-Robert J. Margolis, MD, Center for Health Policy, firstname.lastname@example.org.
Disclaimer: Funding for this meeting was made possible in part by a grant from the U.S. Food and Drug Administration. The views expressed in written conference materials or publications and by speakers and moderators do not necessarily reflect the official policies of the U.S. Food and Drug Administration nor does mention of trade names, commercial practices, or organizations imply endorsements.