HEARING
Discussion Draft of the ‘Food and Drug Administration Globalization Act’ Legislation: Device and Cosmetic Safety Provisions
Subcommittee on Health
Wednesday, May 14, 2008, 10:00 a.m.
2123 Rayburn House Office Building
Hearing Webcast
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Witness List & Prepared Testimony
Please click on the name of the witness to link to their prepared testimony. The testimony is available in Adobe pdf file format.
| Panel I |
|
Stephen Sundlof, D.V.M, Ph.D.
Director
Center for Food Safety and Applied Nutrition
U.S. Food and Drug Administration
5600 Fishers Lane
Rockville, MD 20857
|
Marcia Crosse, Ph.D.
Director, Health Care
U.S. Government Accountability Office
441 G Street, NW, Room 5A14
Washington, DC 20548 |
Lillian Gill, D.P.A.
Senior Associate Director
Center for Devices and Radiological Health
U.S. Food and Drug Administration
5600 Fishers Lane
Rockville, MD 20857
|
|
Panel II
|
|
Mr. Stephen J. Ubl
President and CEO
Advanced Medical Technology Association
701 Pennsylvania Ave., NW, Suite 800
Washington, DC 20004
|
Mr. Kelvyn Cullimore, Jr.
President and CEO
MDMA Secretary
Dynatronics Corporation
7030 Park Centre Drive
Cottonwood Heights, UT 84121 |
Ms. Ami Gadhia
Policy Counsel
Consumers Union
1101 17th Street, NW, Suite 500
Washington, DC 20036
|
Ms. Elisabeth George
Vice President
Quality and Regulatory Affairs
Philips Healthcare
3000 Minuteman Road, Building 1
Andover, MA 01810 |
Ms. Pamela Bailey
President and CEO
Personal Care Products Council
1101 17th Street, NW, Suite 300
Washington, DC 20036
|
Ms. Jane Houlihan
Vice President for Research
Environmental Working Group
1436 U Street N.W., Suite 100
Washington, D.C. 20009 |
Hearing Transcript
Not available at this time. The printed hearing should be available within 90-120 days of the conclusion of the hearing. When available, the text of the printed hearing may be viewed at the U.S. Government Printing Office Web site. |
