Andrew von Eschenbach

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Andrew_von_Eschenbach - HOUSE COMMITTEE EVALUATES FDA ROLE IN DRUG SAFETY ON CAPITOL HILL

HOUSE COMMITTEE EVALUATES FDA ROLE IN DRUG SAFETY ON CAPITOL HILL

FDA Commissioner Andrew von Eschenbach appears before a House Oversight and Government Reform Committee hearing on the safety of the diabetes drug Avandia and the Food and Drug Administration's role in continuing evaluation drugs after they have reached the market, on Capitol Hill in Washington on June 6, 2007. (UPI Photo/Roger L. Wollenberg)


UPI Related News
WASHINGTON, Nov. 18 (UPI) -- The U.S. Food and Drug Administration opened three offices in China this week as part of an effort to improve the safety of food imported from the Asian nation.
FDA: Food protection plan shows progress
WASHINGTON, July 2 (UPI) -- The U.S. Food and Drug Administration says its plan to keep U.S. citizens enjoying one of the safest food supplies in the world shows significant progress.
WASHINGTON, April 9 (UPI) -- The U.S. Food and Drug Administration has appointed Dr. Frank Torti as its principal deputy commissioner and new chief scientist.
WASHINGTON, March 11 (UPI) -- The U.S. Food and Drug Administration has selected Dr. Janet Woodcock to become the agency's director of drug evaluation and research.
WASHINGTON, Oct. 25 (UPI) -- The U.S. Food and Drug Administration announced the creation Thursday of an internal pediatric review committee.
WASHINGTON, Oct. 16 (UPI) -- Gerald Masoudi has been named associate general counsel of the food and drug division of the U.S. Department of Health and Human Services.
WASHINGTON, Oct. 15 (UPI) -- U.S. Food and Drug Administration Commissioner Dr. Andrew von Eschenbach has met with Chinese health officials to discuss the safety of imports.
WASHINGTON, Aug. 23 (UPI) -- The U.S. Food and Drug Administration issued a proposal Thursday setting standards for formulating, testing and labeling over-the-counter sunscreen products.
WASHINGTON, July 25 (UPI) -- The U.S. Food and Drug Administration's Nanotechnology Task Force released a report Wednesday urging the agency consider addressing nanotechnology risks.
WASHINGTON, June 7 (UPI) -- The U.S. Food and Drug Administration is requesting safety warnings for diabetes drugs Avandia and Actos after they came under congressional scrutiny.
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