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On June 16, 2009, the US Food and Drug Administration sent a warning letter to Matrixx Initiatives, manufacturer of an over-the-counter nasal spray for the common cold, Zicam.
Thereafter it ran into Food and Drug Administration (FDA) and judicial obstacles (mainly concerning the methods and viability of the vaccine manufactured by BioPort, a subsidiary of Emergent BioSolutions Inc.).
Health claims for anticarcinogens are regulated by various national and international organizations like the US Food and Drug Administration (FDA) and European Food Safety Authority (EFSA).
In 1978 the U.S. Food and Drug Administration (FDA) external review panel noted that colloidal oatmeal was safe and effective for the symptomatic relief of dry skin and itching.
The non-profit, educational organizations Center for Inquiry (CFI) and the associated Committee for Skeptical Inquiry (CSI) have petitioned the U.S. Food and Drug Administration (FDA), criticizing Boiron for misleading labeling and advertising of Oscillococcinum.
Bosutinib received US FDA and EU European Medicines Agency approval on September 4, 2012 and 27 March, 2013 respectively for the treatment of adult patients with Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML) with resistance, or intolerance to prior therapy.
Four large pharmaceutical companies, Monsanto, American Cyanamid, Eli Lilly, and Upjohn, developed commercial rBST products and submitted them to the US Food and Drug Administration (FDA) for approval.
The film very loosely tracks the history of the real-life breast implant phenomenon, from its radical introduction through its incredible popularity, through the controversial link of its silicone base to various types of illnesses and cancers (culminating in the Food and Drug Administration's moratorium on use of silicone in breast implants, leading the industry to utilize saline ones, instead).
Although the buffet was shut down in 2000 after U.S. Food and Drug Administration inspectors found numerous violations in the galleys of all five vessels, the ship remains an attraction.
Sales reputedly reached $3 million a year, but then the Food and Drug Administration declared the product (and numerous similar products) fraudulent.
Goldin and Katz noted that the birth control pill was approved by the Food and Drug Administration in 1960 for use by married women.
Along with other advocacy groups, such as the International Academy of Oral Medicine and Toxicology, and legislators including Diane Watson (D-CA.) and Congressman Dan Burton (R-IN), Consumers for Dental Choice has called for an investigation of the Food and Drug Administration (FDA) for giving out false and deceptive information about mercury dental fillings, for not issuing warnings to pregnant women, and for failure to advise consumers that dental filling amalgam is mainly mercury.
The United States Food and Drug Administration (FDA), the National Heart, Lung and Blood Institute and the American Heart Association (AHA) all have recommended limiting the intake of trans fats.
Huber received the Commissioner's Special Citation, United States Food and Drug Administration, in recognition of distinguished performance in litigation.
Section 505(j) 21 U.S.C. 355(j) sets forth the process by which would-be marketers of generic drugs can file Abbreviated New Drug Applications (ANDAs) to seek FDA approval of the generic.
The materials used in the production of flexi-bags have to meet the US Food and Drug Administration, EU food-grade or German BGA standards.
In 2003, the United States' CDC and FDA issued an order preventing the importation of the rodents following the first reported outbreak of monkeypox.
In May 2010, the U.S FDA granted Fast Track designation to CDX-011 for the treatment of advanced, refractory or resistant GPNMB-expressing breast cancer.
The U.S. Food and Drug Administration (FDA) Center for Devices and Radiological Health uses it to detect defects in fielded medical devices.
Haw flakes have been seized on several occasions by the United States Food and Drug Administration for containing Ponceau 4R (E124, Acid Red 18), an unapproved artificial coloring.
In Stein's reading, The Wealth of Nations could justify the Food and Drug Administration, the Consumer Product Safety Commission, mandatory employer health benefits, environmentalism and "discriminatory taxation to deter improper or luxurious behavior."
She has been the recipient of the prize for Excellent Design from the Ministry of Housing and Urban-Rural Development and the Ministry of Environmental Protection of the People's Republic of China for her design of Beijing High School No.4.
Depending on when a Hh inhibiting compound is approved by the U.S. Food and Drug Administration (FDA), there may be a perceived need for one to be differentiated over another for marketing purposes, which could lead to different nomenclature (e.g., a Hhi or an agonist of Smo).
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.
The raid wasn't due however to the fact that JLF was selling analogues of then illegal drugs, but rather it was a part of a larger Food and Drug Administration (FDA) crackdown against a large group of herbal medicine providers.
She won FDA approval for a placebo-controlled pilot study on 50 veterans.
In the United States, the Food and Drug Administration allows "langostino" as a market name for three species in the family Galatheidae: Cervimunida johni, Munida gregaria, and Pleuroncodes monodon.
Lupus Center of Excellence physicians also have appointments to advisory committees of the Food and Drug Administration, Alliance for Lupus Research, the Lupus Foundation of America, the American College of Rheumatology and the Arthritis Foundation.
MAKOplasty is a surgical procedure for partial knee or total hip arthroplasty using a RIO Robotic Arm Interactive Orthopedic System developed by MAKO Surgical Corp. RIO is cleared by the FDA for use in surgical knee and hip procedures, in which the use of stereotactic surgery may be appropriate, and where reference to rigid anatomical bony structures can be identified relative to a CT-based model of anatomy.
The northbound direction gains a fourth lane ahead of passing the former Naval Ordnance Laboratory campus to the east, which is now occupied by the Food and Drug Administration.
Middle-of-the-night insomnia is often treated with medication, although currently Intermezzo (zolpidem tartrate sublingual tablets) is the only Food and Drug Administration-approved medication specifically for treating MOTN awakening.
In the context of Food and Drug Administration (FDA) regulation, monographs represent published standards by which the use of one or more substances is automatically authorized.
The Federal Food, Drug and Cosmetic Act (FDCA) requires that all drug manufactures gain approval from the Food and Drug Administration (FDA) before engaging in interstate commerce.
The Food and Drug Administration (FDA) has declared Nambé safe for cooking and serving.
The book gives several examples of government intervention: trade barriers, food and medical regulation, the education system, labor unions, gun control, minimum wage laws, the war on drugs, and advocates of universal health care.
They repeated their actions from the previous week, copying another foot of documents from the District of Columbia Police Department as well as the Food and Drug Administration.
Section 302, the “Authorization for Medical Products for Use in Emergencies” amends the Food and Drug Administration’s (FDA) current Emergency Use Authorization authority to enable the FDA to prepare for and prevent a public health emergency rather than simply responding to it.
After Deniker's observations, they sought and received FDA approval in 1954 to market Thorazine for the treatment of schizophrenia.
The platform includes analytics decision support, collaborative research, and development solutions for drug safety in the Pharma industry and the U.S. Food and Drug Administration (FDA).
The Food and Drug Administration (FDA) states in its review of water pollution that many contaminants survive wastewater treatment and biodegradation, and are detectable in the environment.
News of the incident received publicity in July, 2010 after Miller's daughter, Shirley Sherrod, revealed her version of the events shortly after the controversy surrounding her resignation as Georgia State Director of Rural Development for the United States Department of Agriculture.
They are issued by the U.S. Department of Agriculture, the Food and Drug Administration or the Bureau of Alcohol, Tobacco, Firearms and Explosives.
Having won U.S. Food and Drug Administration approval, the drug is now marketed world-wide as AzilectTM.
The Drug Price Competition and Patent Term Restoration Act (Hatch-Waxman Act) of 1984 provides patent holders on approved patented products with an extended term of protection under the patent to compensate for the delay in obtaining Food and Drug Administration (FDA) approval.
The various sources include the scientific literature, books, government documents, and numerous external databases (such as PubChem, UniProt, PubMed, DrugBank, Human Metabolome Database (HMDB), NIST Chemistry WebBook, KEGG, NCI Database Browser, PharmGKB, Food and Drug Administration, ChEBI, and ChemExper).
Many of the ingredients that they list to be potentially toxic have been found safe by the U.S. Food and Drug Administration (FDA).
This subcommittee has jurisdiction over the budget for the United States Department of Agriculture, Rural Development, and the Food and Drug Administration.
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).
Keeton was the father of former Texas Comptroller and gubernatorial candidate Carole Keeton Strayhorn, and grandfather of Scott McClellan, former White House Press Secretary under U.S. President George W. Bush, and Mark McClellan, who headed the Centers for Medicare and Medicaid Services and was Commissioner of the Food and Drug Administration in the second Bush administration.