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3 Dec 2015, 12:45 pm
Food and Drug Administration (FDA), USDA, and state and local health departments. [read post]
1 Dec 2015, 11:50 am
Xarelto was developed by German pharmaceutical giant Bayer, and is jointly marketed in the United States with Janssen Pharmaceuticals, a division of Johnson & Johnson. [read post]
30 Nov 2015, 10:02 pm
The visit by the Chinese delegation coincided with the Food and Drug Administration’s (FDA) release this past month of the second of two key Food Safety Modernization Act (FSMA) rules that I’ve long argued won’t make our food safer. [read post]
29 Nov 2015, 10:02 pm
FDA is also planning a supplemental notice of proposed rulemaking (NPRM) for “Updating Tolerances for Residues in New Animal Drugs in Food” in April 2016. [read post]
29 Nov 2015, 10:01 pm
Food and Drug Administration (FDA) to treat sesame as a major allergen. [read post]
28 Nov 2015, 9:41 am
It should be noted that when dealing with a highly aggressive deadly form of cancer like mesothelioma, the United States Food and Drug Administration (FDA) will often let pharmaceutical companies fast-track testing, and there is greater tolerance for side effects, since the patient is likely to die without treatment. [read post]
28 Nov 2015, 3:57 am
Attorney’s Office with the Food and Drug Administration – Office of Criminal Investigation. [read post]
27 Nov 2015, 8:59 am
In 2011, the FDA (Food and Drug Administration) approved the blood thinner Xarelto (rivaroxaban) for prescription as an effective anticoagulant. [read post]
27 Nov 2015, 8:59 am
In 2011, the FDA (Food and Drug Administration) approved the blood thinner Xarelto (rivaroxaban) for prescription as an effective anticoagulant. [read post]
27 Nov 2015, 8:29 am
It is estimated that transvaginal mesh is implanted in more than 200,000 women each year in the United States. [read post]
25 Nov 2015, 10:01 pm
Food and Drug Administration (FDA). [read post]
24 Nov 2015, 1:35 pm
Food and Drug Administration, the U.S. [read post]
24 Nov 2015, 1:32 pm
Food and Drug Administration, the U.S. [read post]
24 Nov 2015, 1:26 pm
Food and Drug Administration, the U.S. [read post]
23 Nov 2015, 12:13 pm
During the early 1990s, the company received approval for the drug from the United States Food and Drug Administration (“FDA”) for the limited purposes of treating vomiting and nausea in patients undergoing surgery and chemotherapy. [read post]
23 Nov 2015, 11:33 am
HR 639 would require the DEA to issue an interim final rule to place a drug that has both not been marketed previously in the United States and has abuse potential in a CSA schedule within 90 days of when the drug was approved by the Food and Drug Administration (FDA) when the FDA sends a scheduling recommendation to the DEA, whichever comes later. [read post]
18 Nov 2015, 10:00 am
Food and Drug Administration had only approved Risperdal to treat schizophrenia in adults. [read post]
16 Nov 2015, 10:03 pm
(To sign up for a free subscription to Food Safety News, click here.) [read post]
12 Nov 2015, 10:11 pm
Food & Drug Administration (FDA) announced that for the first time since the passage of the Family Smoking Prevention and Tobacco Control Act of 2009, the agency had cleared new tobacco products for marketing under the statute’s premarket tobacco application pathway, a process that allows tobacco products to be sold in the United States that have not necessarily been deemed safe or “FDA approved. [read post]
12 Nov 2015, 3:20 pm
” See Letter Leslie Kux, Assistant Commissioner for Policy, Food and Drug Administration, to the United States District Court, Northern District of California, dated January 7, 2014. [read post]
