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Food and Drug Administration

The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible for the safety regulation of most types of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics. The FDA also enforces section 361 of the Public Health Service Act and the associated regulations, including sanitation requirements on interstate travel as well as specific rules for control of disease on products ranging from pet turtles to semen donations for assisted reproductive medicine techniques. Read more at Wikipedia


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Analysis of Data from Two Phase 3 Studies Shows DIFICID® Offered Faster Diarrheal Symptom Improvement than Oral Vancomycin in Patients with Cancer Being Treated for Clostridium difficile-Associated Di

...of vancomycin for the treatment of CDAD in adults. These studies served as the basis of approval for DIFICID by the U.S. Food and Drug Administration (FDA) in May 2011. The subpopulation analysis evaluated the treatment of 183 CDAD patients with active cancer...

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    In this Thursday, May 10, 2012 photo, Dr. Lisa Sterman holds up a Truvada pill at her office in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pill’s maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu) (Jeff Chiu) - Published on 2012-05-12 08:39:00 by 13WHAM-TV

    In this Thursday, May 10, 2012 photo, Dr. Lisa Sterman holds up a Truvada pill at her office in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pill’s maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu) (Jeff Chiu)

    Published by 13WHAM-TV on 2012-05-12 08:39:00

    This Thursday, May 10, 2012 photo shows a bottle of Truvada at the office of Dr. Lisa Sterman in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pill’s maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu) - Published on 2012-05-11 13:26:00 by Atlanta Journal Constitution Vendor

    This Thursday, May 10, 2012 photo shows a bottle of Truvada at the office of Dr. Lisa Sterman in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pill’s maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu)

    Published by Atlanta Journal Constitution Vendor on 2012-05-11 13:26:00

    In this Thursday, May 10, 2012 photo, Dr. Lisa Sterman holds up a Truvada pill at her office in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pill’s maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu) - Published on 2012-05-11 08:31:00 by Atlanta Journal Constitution Vendor

    In this Thursday, May 10, 2012 photo, Dr. Lisa Sterman holds up a Truvada pill at her office in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pill’s maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu)

    Published by Atlanta Journal Constitution Vendor on 2012-05-11 08:31:00

    In this Thursday, May 10, 2012 photo, Dr. Lisa Sterman holds up a Truvada pill at her office in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pillâÃÂÃÂs maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu) - Published on 2012-05-11 04:36:00 by Wilkes-Barre Weekender

    In this Thursday, May 10, 2012 photo, Dr. Lisa Sterman holds up a Truvada pill at her office in San Francisco. Sterman prescribes the drug off-label for about a dozen patients at high risk for developing AIDS. The pill, already used to treat people with HIV, also helps prevent the virus from infecting healthy people. The Food and Drug Administration is expected to decide by June 15 whether the pillâÃÂÃÂs maker Gilead Sciences should be allowed to formally market the drug for preventive use. (AP Photo/Jeff Chiu)

    Published by Wilkes-Barre Weekender on 2012-05-11 04:36:00

    The U.S. Food and Drug Administration (FDA) Antiviral Drugs Advisory Committee holds a meeting to vote on whether Gilead Sciences' Truvada should be approved as a preventative treatment for people who are at high risk of contracting HIV through sexual intercourse May 10, 2012 in Silver Spring, Maryland. Already approved to treat people infected with HIV, Truvada would be a milestone in the worldwide AIDS epidemic by offering a tablet capable of preventing infection in high-risk individuals. - Published on 2012-05-10 19:01:00 by Montreal Gazette

    The U.S. Food and Drug Administration (FDA) Antiviral Drugs Advisory Committee holds a meeting to vote on whether Gilead Sciences' Truvada should be approved as a preventative treatment for people who are at high risk of contracting HIV through sexual intercourse May 10, 2012 in Silver Spring, Maryland. Already approved to treat people infected with HIV, Truvada would be a milestone in the worldwide AIDS epidemic by offering a tablet capable of preventing infection in high-risk individuals.

    Published by Montreal Gazette on 2012-05-10 19:01:00

    The U.S. Food and Drug Administration (FDA) Antiviral Drugs Advisory Committee holds a meeting to vote on whether Gilead Sciences' Truvada should be approved as a preventative treatment for people who are at high risk of contracting HIV through sexual intercourse May 10, 2012 in Silver Spring, Maryland. Already approved to treat people infected with HIV, Truvada would be a milestone in the worldwide AIDS epidemic by offering a tablet capable of preventing infection in high-risk individuals. - Published on 2012-05-10 18:46:00 by Vancouver Sun

    The U.S. Food and Drug Administration (FDA) Antiviral Drugs Advisory Committee holds a meeting to vote on whether Gilead Sciences' Truvada should be approved as a preventative treatment for people who are at high risk of contracting HIV through sexual intercourse May 10, 2012 in Silver Spring, Maryland. Already approved to treat people infected with HIV, Truvada would be a milestone in the worldwide AIDS epidemic by offering a tablet capable of preventing infection in high-risk individuals.

    Published by Vancouver Sun on 2012-05-10 18:46:00

    The U.S. Food and Drug Administration (FDA) Antiviral Drugs Advisory Committee holds a meeting to vote on whether Gilead Sciences' Truvada should be approved as a preventative treatment for people who are at high risk of contracting HIV through sexual intercourse May 10, 2012 in Silver Spring, Maryland. Already approved to treat people infected with HIV, Truvada would be a milestone in the worldwide AIDS epidemic by offering a tablet capable of preventing infection in high-risk individuals. - Published on 2012-05-10 18:39:00 by Canada.com

    The U.S. Food and Drug Administration (FDA) Antiviral Drugs Advisory Committee holds a meeting to vote on whether Gilead Sciences' Truvada should be approved as a preventative treatment for people who are at high risk of contracting HIV through sexual intercourse May 10, 2012 in Silver Spring, Maryland. Already approved to treat people infected with HIV, Truvada would be a milestone in the worldwide AIDS epidemic by offering a tablet capable of preventing infection in high-risk individuals.

    Published by Canada.com on 2012-05-10 18:39:00

    The U.S. Department of Health and Human Services building which houses the Food and Drug Administration (FDA) in Rockville, MD. (Getty Images) - Published on 2012-05-10 13:34:00 by 13WHAM-TV

    The U.S. Department of Health and Human Services building which houses the Food and Drug Administration (FDA) in Rockville, MD. (Getty Images)

    Published by 13WHAM-TV on 2012-05-10 13:34:00

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    The bottom line is that the goal of our laws and policies for medicines must be to develop drugs as quickly as possible, drugs that are the most effective we can find for the diseases people are facing, and to get them out to every person who needs them as soon as possible...

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