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31 Oct 2016, 10:00 pm by Coral Beach
” Officials with the Food and Drug Administration posted the Egyptian company’s recall notice Monday, but are barred by corporate confidentiality clauses in federal law from revealing the company’s customers or volumes of strawberries involved. [read post]
31 Oct 2016, 4:32 pm by Bill Marler
The Food and Drug Administration’s recall announcement, dated Sunday, stated that the company’s action was taken in consultation with FDA because the Hepatitis A virus was detected in four lots of frozen strawberries ICAPP exported to the U.S. [read post]
31 Oct 2016, 9:22 am by Cathy Siegner
The Food and Drug Administration’s recall announcement, dated Sunday, stated that the company’s action was taken in consultation with FDA because the Hepatitis A virus was detected in four lots of frozen strawberries ICAPP exported to the U.S. [read post]
31 Oct 2016, 7:51 am by Attorney Bert Louthian
As of August, 2016, the Food and Drug Administration (FDA) now has the authority to regulate ENDS, or Electronic Nicotine Delivery Systems. [read post]
31 Oct 2016, 7:18 am by Robert Kraft
in-Pharma Technologist reports that Food and Drug Administration commissioner Dr. [read post]
31 Oct 2016, 5:00 am by Christopher Hoffmann
Precautions When Using Antihistamines The Food and Drug Administration recommends the following precautions when taking antihistamines: Be careful about the dosage of antihistamines. [read post]
30 Oct 2016, 10:01 pm by News Desk
One allergic reaction had been reported in the United States or its territories, where the Oreo cookies were distributed, as of the Friday posting of the recall notice on the Food and Drug Administration’s website. [read post]
29 Oct 2016, 7:55 am by Law Offices of Jeffrey S. Glassman
  While you might think this would be enough to get Xarelto and its classmates taken off the market, that has not been the case, despite some newer warnings from the United States Food and Drug Administration (FDA). [read post]
28 Oct 2016, 2:35 pm by Laura Ray
Food and Drug Administration (FDA) under a New Drug Application, has patent protection, and has no FDA-approved therapeutic equivalents – it is a single source or brand drug, not a multiple source or generic drug. [read post]
28 Oct 2016, 1:14 pm by Kit Walsh
To evaluate the “response” of other agencies, EFF submitted Freedom of Information Act requests to the Environmental Protection Agency, the Food and Drug Administration, the Department of Transportation, and the California Air Resources Board, asking for records of any action they were taking in response to the DMCA exemptions, and any record that they relied upon the DMCA in regulating their domains. [read post]
27 Oct 2016, 10:00 pm by Jared Zola & James Murray
The FSMA gives the Food and Drug Administration legislative authority to create and police preventative control standards. [read post]
27 Oct 2016, 9:30 pm by Justin Daniel
Food and Drug Administration (FDA) released a set of draft guidelines on how tobacco manufacturers can comply with rules requiring that they list the ingredients in tobacco products. [read post]
27 Oct 2016, 10:06 am by Law Offices of Jeffrey S. Glassman
 Food and Drug Administration (FDA) to warn of the dangers of these products, and they were soon largely taken off the market. [read post]
27 Oct 2016, 8:00 am by Sevens Legal
Party hosts need to be ready with non-alcoholic drinks, food, and the responsibility to make sure their guests get home safely. [read post]
27 Oct 2016, 3:14 am by Cari Rincker
In June 2015, the Food & Drug Administration (“FDA”) promulgated the second Veterinary Feed Directive (“VFD”) affecting livestock producers that use medicated feed and water. [read post]
26 Oct 2016, 10:01 pm by News Desk
No bobbing zoneSafeguarding against bacteria from apples — and party goers — in bobbing tubs is easy, according to tips offered by the Food and Drug Administration and the food safety advocacy group FightBAC.org, which stands for Fight Bacteria. [read post]
26 Oct 2016, 1:04 pm by Debra A. McCurdy and Yetunde Oni
The Food and Drug Administration (FDA) and the Centers for Medicare & Medicaid Services (CMS) have announced that they are making permanent their “Program for Parallel Review of Medical Devices,” which is now operating as a pilot program. [read post]
25 Oct 2016, 9:30 pm by Thomas D. Campbell
Food and Drug Administration (FDA) is seeking to answer just that question. [read post]