In 1964, Surgeon General Luther Terry issued a report on smoking and health saying that tobacco causes lung cancer and is a main contributor to bronchitis.
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In March 2008, major recalls of heparin, a substance widely used as an injectable anticoagulant, were announced by the U.S. Food and Drug Administration (FDA) due to contamination of the raw heparin stock imported from China.
These agencies distinguish themselves through an understanding of the strict labeling and marketing guidelines mandated by the U.S. Food and Drug Administration (FDA) and industry group guidelines, notably ADVAMED and PHARMA.
In 2008, the U.S. Food and Drug Administration determined that absinthe was legal, though it had been understood to be illegal for about 80 years.
Discovered by Dr. Baldomero Olivera at University of Utah, it was developed for treatment of chronic and intractable pain caused by AIDS, cancer, neurological disorders and other maladies, and was approved by the U.S. Food and Drug Administration in December 2004 under the name Prialt.
As of 2008, the U.S. Food and Drug Administration (FDA) was planning a study to see if coupons make patients overlook drug risks and side effects in their effort to save money.
On April 5, 2013, Judge Edward R. Korman in Brooklyn, New York, ordered the U.S. Food and Drug Administration to make the morning-after birth control pill available to people of any age without a prescription.
The U.S. Food and Drug Administration (FDA) warns to be aware of the potential of foreign packages, which may come from gang printing at the package supplier.
The merged company as Picker International had the first MRI scanner approved by the U.S. Food and Drug Administration (FDA) on the US market.
In 1992, Burkey Belser was contacted by David Aaron Kessler's staff at the U.S. Food and Drug Administration to help with the Nutrition Facts label because of his prior success designing the EnergyGuide that appears on all major appliances in the United States.
The U.S. Food and Drug Administration (FDA), and U.S. Federal Communications Commission (FCC) set limits for the amounts of Radio Frequency Energy exposure permitted in a standard work-day.
Rosa Delia Valenzuela had been taking the doctor-prescribed drug Rezulin that a few months later was withdrawn from the market when the U.S. Food and Drug Administration concluded that Rezulin use had "possibly or probably" resulted in 90 liver failures, including 63 deaths and seven nonfatal organ transplants.
Ms. Doswell later began a career with the U.S. Food and Drug Administration in 1985, serving as a seafood inspector in FDA's Los Angeles District, San Pedro, California.
Linda Andre is an American psychiatric survivor activist and writer, living in New York City, who is the director of the Committee for Truth in Psychiatry (CTIP), an organization founded by Marilyn Rice in 1984 to encourage the U.S. Food and Drug Administration (FDA) to regulate ECT (electroconvulsive therapy) machines.
According to USAMRIID, the Whitecoat operation contributed to vaccines approved by the U.S. Food and Drug Administration (FDA) for yellow fever and hepatitis, and investigational drugs for Q fever, Venezuelan equine encephalitis, Rift Valley fever, and tularemia.
He performed the viral load testing for Merck data submission to the U.S. Food and Drug Administration for approval of Crixivan.
The U.S. Food and Drug Administration has approved rivastigmine capsules and patches for the treatment of mild to moderate dementia of the Alzheimer’s type and for mild to moderate dementia related to Parkinson's disease.
In 2009 the U.S. FDA published draft guidance for the pharmaceutical industry to use serial numbers on prescription drug packages.
As of February 15, 2013, all of the top 20 pharmaceutical companies, along with the U.S. Food and Drug Administration (FDA), the Centers for Disease Control and Prevention (CDC), the National Institutes of Health (NIH), and the National Cancer Institute (NCI) license the company's software.
Sucralfate was approved by the U.S. Food and Drug Administration (FDA) in 1981.
From 1993–1997 she served as the consumer representative on the U.S. Food and Drug Administration’s Obstetrics and Gynecology Devices Advisory Panel.
As a member of the Association of Health Care Journalists, she requested with other journalists that the U.S. Food and Drug Administration (FDA) end current practices that restrict the public's access to health information.
They also found that the U.S. Food and Drug Administration (FDA) failed to remove several drugs already known to be carcinogens.
The U.S. Food and Drug Administration then issued an advisory against consuming tomalley from American lobster found anywhere in the Atlantic Ocean.
This subcommittee has jurisdiction over the budget for the United States Department of Agriculture, Rural Development, and the Food and Drug Administration.
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This subcommittee has jurisdiction over the Department of Agriculture discretionary spending (does not include the Food Stamp Program or farming subsidies that are mandatory spending), as well as food safety programs at the Food and Drug Administration and foreign agriculture assistance programs.
Certain agencies within Health and Human Services are handled by separate subcommittees, such as the Indian Health Service (Interior Subcommittee) and the Food and Drug Administration (Agriculture Subcommittee).
Her past affiliations include the U.S. Food and Drug Administration's Center for Drug Evaluation and Research, and Genentech.
Horwitz worked for the U.S. Food and Drug Administration (FDA) for 57 years until his retirement in 2000 and was head of the Association of Official Analytical Chemists for 24 years.
In the final decade of his life, Winslow Carlton co-founded and served as president of Selcore Labs, where a new a-cellular pertussis vaccine was developed and approved by the U.S. Food and Drug Administration.