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Food and Drug Administration print that page

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The Food and Drug Administration ( FDA or USFDA ) is an agency of the United States Department of Health and Human Services , one of the United States federal executive departments . The FDA is responsible for protecting and promoting public health through the regulation and supervision

Criticism of the Food and Drug Administration print that page

Foods

Numerous governmental and non-governmental organizations have criticized the U. S. Food and Drug Administration of either over- or under- regulation . The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible

National Agency for Food and Drug Administration and Control print that page

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General : Paul Bortwev Orhii Headquarters : Abuja , Nigeria The National Agency for Food and Drug Administration and Control (NAFDAC) is a Nigerian government agency under the Federal Ministry of Health that is responsible for regulating and controlling the manufacture, importation

Drug Enforcement Administration print that page

DEA-Agents.

The Drug Enforcement Administration ( DEA ) is a federal law enforcement agency under the United States Department of Justice , tasked with combating drug smuggling and use within the United States . Not only is the DEA the lead agency for domestic enforcement of the Controlled Substances

Comprehensive Drug Abuse Prevention and Control Act of 1970 print that page

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The Comprehensive Drug Abuse Prevention and Control Act of 1970 , Pub. L. No. 91-513, 84 Stat. 1236 (Oct. 27, 1970), is a United States federal law that, with subsequent modifications, requires the pharmaceutical industry to maintain physical security and strict record keeping for certain

Food and Drug Administration Modernization Act of 1997 print that page

The United States Food and Drug Administration Modernization Act of 1997 (FDAMA) amended the Federal Food, Drug , and Cosmetic Act . This act is related to the regulation of food, drugs, devices, and biological products by the FDA . These changes were made in order to recognize the changes

wikipedia.org | 2011/7/2 15:26:01

Prescription Drug User Fee Act print that page

The Prescription Drug User Fee Act (PDUFA) was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration (FDA) to collect fees from drug manufacturers to fund the new drug approval process. The Act provided that the FDA was entitled to collect

wikipedia.org | 2011/5/9 8:21:56

Federal Food, Drug, and Cosmetic Act print that page

The United States Federal Food, Drug , and Cosmetic Act (abbreviated as FFDCA , FDCA , or FD&C ), is a set of laws passed by Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food , drugs, and cosmetics. A principal author of this

wikipedia.org | 2011/9/20 6:42:35

Center for Food Safety and Applied Nutrition print that page

The Center for Food Safety and Applied Nutrition (CFSAN, pronounced sif'-san) is the branch of the United States Food and Drug Administration (FDA) that regulates food, dietary supplements , and cosmetics [ citation needed ] . Contents 1 Area of regulation 1.1 Areas of concern

wikipedia.org | 2011/3/25 8:35:48

Patient safety organization print that page

Patients for Patient Safety (PfPS) 2.2 Australia and New Zealand 2.2.1 Therapeutic Goods Administration and Adverse Drug Reactions Advisory Committee 2.2.2 Australian Commission on Safety and Quality in Health Care 2.3 United Kingdom 2.3.1 National Patient Safety Agency 2

wikipedia.org | 2011/5/3 19:30:53