Food and Drug Administration

Food and Drug Administration Newswire (Page 2)

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Results 21 - 40 of 32,205 in Food and Drug Administration

  1. Over 1,500 industry, government and academic professionals attended last week's Food Safety SummitRead the original story

    3 hrs ago | National Provisioner

    Attendees to last week's Food Safety Summit had the opportunity to participate in timely workshops, informative sessions and network with 178 vendors who provide products and services to help food safety professionals do their job more effectively and efficiently.

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  2. Nanticoke Patient First in Delaware to Receive TreatmentRead the original story w/Photo

    3 hrs ago | Cape Gazette

    ... Nanticoke Cardiology. Cardiovascular Systems, Inc. (CSI) received PMA approval from the U.S. Food and Drug Administration (FDA) to market its Diamondback 360 Coronary Orbital Atherectomy System (OAS) as a treatment for severely calcified coronary ...

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  3. Idera CEO says momentum remains strong despite stock declinesRead the original story

    3 hrs ago | Business Journal

    ... of patients. That trial could form the basis of an application for approval to the U.S. Food and Drug Administration, with the best case scenario of the drug being approved for that disease sometime in 2017. There are plenty of other reasons for ...

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  4. United States brand name pharmaceutical manufacturing market: $176.7 billion industry by 2018Read the original story w/Photo

    3 hrs ago | PR-inside.com

    ... drugs. The Patient Protection and Affordable Care Act of 2010 introduced a method for the US Food and Drug Administration to approve generic biologics, but also initiated a 12-year patent period on these types of drugs. While this legislation ...

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  5. The Growth Strategies of Israel's Burgeoning Medical Device SectorRead the original story

    3 hrs ago | Knowledge@Wharton

    ... people with lower limb disabilities to walk. It was the first to reach the market with a U.S. Food and Drug Administration-approved device for rehabilitation centers, though the company's investment was one-third that of the competition, Perry ...

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  6. 17-Day Leech Treatment Helps Save Woman's Ear After Dog AttackRead the original story w/Photo

    3 hrs ago | Health.com

    ... but at the same time this is not a commonly performed procedure," he noted. "The FDA [U.S. Food and Drug Administration] approved leeches in 2004 for all sorts of amputation situations, with a detached finger probably being the most common type of ...

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  7. Most Medical Devices for Kids Only Tested on AdultsRead the original story w/Photo

    3 hrs ago | Health.com

    ... in clinical trials, the researchers report. "Many devices that are approved by the U.S. Food and Drug Administration for use in children have had only very limited study in actual pediatric patients," said lead researcher Dr. Florence Bourgeois, a ...

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  8. Maryland's abandoned health exchange had no discernible leadershipRead the original story

    4 hrs ago | Business Journal

    ... marketplaces. The state's health secretary, a long-time health care leader who left the Food and Drug Administration to head Maryland's health department, played a big role fleshing out the new agency. And the governor tasked his second-in-command, ...

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  9. With launch of new epilepsy drug, Sunovion already aiming at expanded approvalRead the original story

    4 hrs ago | Business Journal

    ... that was named Sepracor before the 2012 acquisition, got approval for the drug from the U.S. Food and Drug Administration last November. Russell said that in the last five months, the company hired a 120-person global sales force and worked on the ...

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  10. Shareholder Alert: Pomerantz Law Firm Announces the Filing of a Class ...Read the original story

    4 hrs ago | Sys-Con Media

    ... did not show superiority to clopidogrel, a competing drug already approved by the U.S. Food and Drug Administration ("FDA"); (2) The Company's CHAMPION clinical trials which compared the efficacy of Cangrelor to clopidogrel were unethically and ...

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  11. In Case You Missed It: GlaxoSmithKline Just Had a Phenomenal WeekRead the original story w/Photo

    5 hrs ago | The Motley Fool

    ... phenomenal week It all began on Tuesday, when GlaxoSmithKline announced that the Food and Drug Administration had approved its subcutaneous, once-weekly type 2 diabetes therapy Tanzeum as an adjunct to proper diet and exercise. Tanzeum is a GLP-1 ...

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  12. Cycling and walking benefits; anti-vaccine movement ills: Healthy LivingRead the original story w/Photo

    5 hrs ago | OregonLive.com

    ... fibroids. The procedure poses a risk of spreading cancerous tissue, according to the U.S. Food and Drug Administration. ( New York Times ) MORNING SICKNESS DRUG: Pyridoxine-doxylamine, the most commonly prescribed drug for first trimester morning ...

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  13. As allergy season ramps up, new pill receives FDA approvalRead the original story w/Photo

    5 hrs ago | WLWT-TV Cincinnati

    ... of allergy shots doesn't sound much better, there's a new remedy on the horizon, the newly U.S. Food and Drug Administration approved grass allergy pill, Grastek. Allergist and immunologist Dr. David Bernstein is one of the clinical researchers for ...

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  14. Quitting smoking using e-cigarettes might not work, researchers sayRead the original story

    5 hrs ago | Star Tribune

    ... uit is contradictory and inconclusive." E-cigarettes, he wrote, should be regulated by the U.S. Food and Drug Administration "as a drug-delivery device."

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  15. Medical groups tell doctors to weigh costs of drugs when prescribingRead the original story

    5 hrs ago | Anchorage Daily News

    ... year if everyone used the cheaper drug, Avastin, instead of the costlier one, Lucentis. But the Food and Drug Administration has not approved Avastin for use in the eye; and using it rather than the alternative, Lucentis, might carry an additional, ...

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  16. Sisters hope iTan salon sets a tone in San ClementeRead the original story

    5 hrs ago | OC Community Network

    Hours: 7 a.m. to 9 p.m. Mondays through Fridays, 8 a.m. to 9 p.m. Saturdays, 8 a.m. to 8 p.m. Sundays Though iTan's salon staff is trained to give clients a safe amount of exposure to ultraviolet rays, the U.S. Food and Drug Administration cautions that "exposure to UV radiation, whether from the sun or indoor tanning beds, can cause skin cancer ,

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  17. Provillus Hair Regrowth Treatment Product Available for Men and Women with 1 Free Bottle OfferRead the original story

    5 hrs ago | SBWire

    Currently, there are over 35 million US men and 21 million US women experiencing hair loss, with devastating results for the sufferers' emotional state and self image.

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  18. Continue reading a 'Read the original story

    6 hrs ago | Grocery Headquarters

    The Grocery Manufacturers Association has issued the following statement in response to the movement of HB 112, a bill that would require mandatory labeling of foods containing genetically modified ingredients, through the Vermont legislature: "Vermont HB 112 is a step in the wrong direction for consumers.

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  19. Glenmark Pharmaceuticals recalls stomach ulcer drug ranitidine in USRead the original story w/Photo

    6 hrs ago | Express India

    ... and over-the-counter drugs sold in the United States, have come under increased scrutiny by the Food and Drug Administration over the past year. In the last six months alone, products made by some of India's largest drugmakers, including Ranbaxy ...

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  20. Ragwitek Approved for Adult Ragweed AllergyRead the original story

    7 hrs ago | Drugs.com

    FRIDAY April 18, 2014, 2014 -- Ragwitek has been approved by the U.S. Food and Drug Administration to treat allergy to short ragweed among adults aged 18 to 65. The once-daily tablet contains an extract from short ragweed pollen, the agency said in a news release.

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