HEARING
Discussion Draft of the ‘Food and Drug Administration Globalization Act’ Legislation: Drug Safety
Subcommittee on Health
Thursday, May 1, 2008, 10:00 a.m.
2322 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 |
|
Janet Woodcock, M.D.
Director
Center for Drug Evaluation and Research
Food and Drug Administration
5600 Fishers Lane
Rockville, MD 20857
|
|
Panel II
|
|
Mr. William K. Hubbard
Senior Advisor
Coalition for a Stronger FDA
202 Weaver Mine Trail
Chapel Hill, NC 27517
|
Ms. Lori Reilly
Vice President of Policy
The Pharmaceutical Research and Manufacturers of America
950 F Street, NW
Washington, DC 20004 |
The Honorable James C. Greenwood
President and CEO
Biotechnology Industry Organization
1201 Maryland Avenue, SW, Suite 900
Washington, DC 20024
|
Ms. Christine Mundkur
Chief Executive Officer
Barr Laboratories, Inc.
25 Massachusetts Ave., NW,
Suite 440
Washington, DC 20001 |
Mr. Ron Bone
Senior Vice President, Distribution Support
McKesson Corporation
One Post Street
San Francisco, CA 94104
|
Kevin Nicholson, R.Ph., J.D.
Vice President
Pharmacy Regulatory Affairs
National Association of Chain Drug Stores
413 North Lee Street
Alexandria, VA 22314 |
Ms. Ami Gadhia
Policy Counsel
Consumers Union
1101 17th Street, NW, Suite 500
Washington, DC 20036
|
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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. |
