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June 28, 2000

Regulation of Over the Counter Drugs Day 1

Health experts and industry lobbyists debated the extent to which prescription drugs should be converted to “over the counter” status. They… read more

Health experts and industry lobbyists debated the extent to which prescription drugs should be converted to “over the counter” status. They also talked about the sometimes blurry line between cosmetics and drugs. This program contains several short breaks. close

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Amy Alhna Program Director National Women's Health Network
Eva Bachrach Senior Vice President Consumer Healthcare Products Association

Russell Bantham Deputy Counsel Pharmaceutical Research and Manufacturers of America
Anthony Barrueta Counsel Kaiser Permanente->Government Relations
David Bradford Professor University of Utah->School of Medicine
Schumarry Chao Representative MEDIMPACT
Rebecca Chater Representative American Pharmaceutical Association
Robert DeLap Director U.S. Food and Drug Administration->Center for Drug Evaluation and Research
Thomas Donegan Vice President Cosmetic, Toiletry and Fragrance Assn.
Gerald Dunaway President AMMSYS Research, Inc.
Steve Francesco President Francesco International
Charles Ganley Director U.S. Food and Drug Administration->Nonprescription Drugs Cmte.
Linda Golodner President National Consumers League
Michael Greene Representative American College of Obstetricians and Gynecologists
Doug Hoey Vice President National Community Pharmacists Assn.
Mary Johnson Attorney
Dr. Chris Kahlenborn Participant
Brett Kay Program Associate National Consumers League
James Leyden Professor University of Pennsylvania School of Medicine
Anna Longwell Director Becton, Dickinson, and Company->Corporate Regulatory Affairs
Michael Maves President Consumer Healthcare Products Association
Warren Pinchert II President and CEO Cholestech Corporation
Robert Pinco Attorney
William Soller Senior Vice President Consumer Healthcare Products Association
Robert Temple Associate Director U.S. Food and Drug Administration->Office of Drug Evaluation
Sandra Titus Executive Secretary Nonprescription Drugs Advisory Committee
Sidney Wolfe M.D. Co-Founder and Director Public Citizen->Health Research Group
Janet Woodcock M.D. Official U.S. Food and Drug Administration

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U.S. Food and Drug AdministrationU.S. Food and Drug Administration

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Program ID:: 157953-1
Category:: Public Affairs Event
Format:: Public Hearing
Location:: Washington, District of Columbia, United States
First Aired:: Jun 28, 2000 | 11:33pm EDT | C-SPAN 2

Airing Details

Jun 28, 2000 | 11:33pm EDT | C-SPAN 2

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June 28, 2000
Reg. of Over the Ctr. Drugs
- 2 minutes
- 22 views