For Food And Drug Administration (Fda) we have terms and definitions in 12 topics. The topics are Addiction, Animal Health, Clinical Trials, Colon Cancer, Drug Trials, Food and Health, HIV and AIDs, Health Care, Hepatitis B, Law, Multiple Sclerosis and Oncology.

Food And Drug Administration (Fda) (Addiction)

Agency of the U.S. Department of Health and Human Services that administers federal laws regarding the purity of food, the safety and effectiveness of drugs and the safety of cosmetics.

Food And Drug Administration (Fda) (Animal Health)

Federal agency, under the Department of Health and Human Services, that regulates the development, approval and surveillance of food, drugs and cosmetics.

Food And Drug Administration (Fda) (Clinical Trials)

The U.S. Department of Health and Human Services agency responsible for ensuring the safety and effectiveness of all drugs, biologics, vaccines, and medical devices, including those used in the diagnosis, treatment, and prevention of HIV infection, AIDS, and AIDS-related opportunistic infections. The FDA also works with the blood banking industry to safeguard the nation's blood supply. Internet address: http://www.fda.gov/.

Food And Drug Administration (Fda) (Colon Cancer)

The FDA’s role is to oversee the pharmaceutical research conducted by drug companies, university research centers and physicians to make sure that federal regulations governing this research are followed.

Food And Drug Administration (Fda) (Drug Trials)

The FDA is responsible for protecting the public health by assuring the safety, efficacy, and quality of drugs, biologics and many other medical products. The FDA is also responsible for advancing the public health by helping to speed innovations that make medicines more effective, safer, and more affordable; and helping the public get the accurate, science-based information they need to use medicines to improve their health. More information is available at www.fda.gov.

Food And Drug Administration (Fda) (Food and Health)

The Food and Drug Administration is part of the Public Health Service of the U.S. Department of Health and Human Services. It is the regulatory agency responsible for ensuring the safety and wholesomeness of all foods sold in interstate commerce except meat, poultry and eggs (which are under the jurisdiction of the U.S. Department of Agriculture). FDA develops standards for the composition, quality, nutrition, safety and labeling of foods including food and color additives. It conducts research to improve detection and prevention of contamination. It collects and interprets data on nutrition, food additives and pesticide residues. The agency also inspects food plants, imported food products and feed mills that make feeds containing medications or nutritional supplements that are destined for human consumption. And it regulates radiation-emitting products such as microwave ovens. FDA also enforces pesticide tolerances established by the Environmental Protection Agency for all domestically produced and imported foods, except for foods under USDA jurisdiction.

Food And Drug Administration (Fda) (HIV and AIDs)

An agency of the United States Department of Health and Human Services. Aside from regulating the safety of foods and cosmetics, the FDA regulates the testing of EXPERIMENTAL DRUGS and approves new medical products for marketing based on evidence of safety and EFFICACY.

Food And Drug Administration (Fda) (Health Care)

An agency within the Federal government that is responsible for regulations pertaining to food and drugs sold in the United States.

Food And Drug Administration (Fda) (Hepatitis B)

A federal organization charged with protecting the public health. It establishes safety and effectiveness guidelines for healthcare products such as the drugs that are used to treat hepatitis B and C.

Food And Drug Administration (Fda) (Law)

A federal agency which sets safety and quality standards for Administration food, drugs, cosmetics, and household substances.

Food And Drug Administration (Fda) (Multiple Sclerosis)

The U.S. federal agency that is responsible for enforcing governmental regulations pertaining to the manufacture and sale of food, drugs, and cosmetics. Its role is to prevent the sale of impure or dangerous substances. Any new drug that is proposed for the treatment of MS in the United States must be approved by the FDA.

Food And Drug Administration (Fda) (Oncology)

The United States Food and Drug Administration (FDA) is a public health agency, charged with protecting U.S. consumers by enforcing the Federal Food, Drug, and Cosmetic Act and related public health laws. In deciding whether to approve new drugs, the FDA itself does not conduct research; rather it examines the results of studies conducted by the manufacturer. The FDA must determine that the new drug produces the expected benefits without causing side effects that outweigh those benefits.

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