News & Events
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Congressional Testimony 2011
This section includes testimony by FDA officials before House and Senate Committees and Subcommittees.
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December 2011
- 12/15/2011
Prescription Drug Shortages: Examining a Public Health Concern and Potential Solutions
Sandra Kweder, M.D., before the Senate Committee on Health, Education, Labor and Pensions
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November 2011
- 11/15/2011
Medical Devices: Protecting Patients and Promoting Innovation
Jeffrey Shuren, M.D., J.D., before the Senate Committee on Health, Education, Labor and Pensions
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September 2011
- 09/14/2011
Securing the Pharmaceutical Supply Chain
Deborah M. Autor, Esq., before the Senate Committee on Health, Education, Labor and Pensions - 09/13/2011
Agro-Defense: Responding to Threats Against America's Agriculture and Food System
Ted Elkin, before the Senate Committee on Homeland Security and Governmental Affairs, Subcommittee on Oversight of Government Management, the Federal Workforce, and the District of Columbia
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July 2011
- 07/28/2011
FDA User Fees: Advancing Public Health
Margaret A. Hamburg, M.D., before the Senate Committee on Health, Education, Labor, and Pensions - 07/20/2011
Regulatory Reform Series #5 - FDA Medical Device Regulation: Impact on American Patients, Innovation and Jobs
Jeffrey Shuren, M.D., J.D., before the House Committee on Energy and Commerce, Subcommittee on Oversight and Investigations - 07/07/2011
PDUFA V: Medical Innovation, Jobs, and Patients
Janet Woodcock, M.D., before the House Committee on Energy and Commerce, Subcommittee on Health
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June 2011
- 06/22/2011
Transforming Lives Through Diabetes Research
Charles Zimliki, Ph.D., before the Senate Committee on Homeland Security and Governmental Affairs - 06/02/2011
Pathway to FDA Medical Device Approval: Is There a Better Way?
Jeffrey Shuren, M.D., J.D., before the House Committee on Oversight and Government Reform, Subcommittee on Health Care, District of Columbia, Census and the National Archives
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May 2011
- 05/03/2011
Sacred Obligation: Restoring Veteran Trust and Patient Safety
Anthony D. Watson, B.S., M.S., M.B.A., before the House Committee on Veterans' Affairs
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April 2011
- 04/13/2011
A Delicate Balance: FDA and the Reform of the Medical Device Approval Process
William Maisel, M.D., M.P.H., before the Senate Special Committee on Aging - 04/13/2011
Import Safety: Status of FDA's Screening Efforts at the Border
Margaret A. Hamburg, M.D., before the House Committee on Energy and Commerce, Subcommittee on Oversight and Investigations
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March 2011
- 03/11/2011
The President’s Fiscal Year 2012 Budget Request for FDA
Margaret A. Hamburg, M.D., before the House Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies
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February 2011
- 02/17/2011
Impact of Medical Device Regulation on Jobs and Patients
Jeffrey Shuren, M.D., J.D., before the House Committee on Energy and Commerce, Subcommittee on Health
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