Search for: "UNITED STATES FOOD & DRUG ADMINISTRATION " Results 2981 - 3000 of 6,135
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12 Nov 2015, 11:30 am by John Elwood
First up, a tangle of one-time relists, all concerning the validity of the Obama administration’s efforts to accommodate religious objections to the Affordable Care Act’s regulatory requirement that employer-provided health care programs make available all contraceptives approved by the Food and Drug Administration. [read post]
11 Nov 2015, 1:32 pm by Clay Hodges
 Zimmer sent an “Urgent Medical Device Recall” letter to surgeons and risk managers, and then notified the Food and Drug Administration. [read post]
5 Nov 2015, 3:32 am by Bill Marler
Food and Drug Administration (FDA) to investigate a multistate outbreak of Listeria monocytogenes infections (listeriosis). [read post]
4 Nov 2015, 9:34 am by Law Offices of Jeffrey S. Glassman
According to a recent news article from the Washington Post, a federal watch group reports the United States Food and Drug Administration (FDA) exercised “lax” judgment and made “questionable” decisions to be accommodating to the pharmaceutical maker Boehringer Ingelheim when reviewing its application for the anticlotting medication known as Pradaxa. [read post]
3 Nov 2015, 11:40 am
The United States Department of Health and Human Services Office of Inspector General ("HHS-OIG") has released its Work Plan for Fiscal Year 2016. [read post]
2 Nov 2015, 9:31 am by Zachary K. Goldman, Ramesh Karri
 And we entrust the Food and Drug Administration to ensure that medical device companies only introduce products into the marketplace after they have been tested thoroughly, in accordance with widely-accepted standards. [read post]
1 Nov 2015, 9:33 am by Law Offices of Jeffrey S. Glassman
The United States Food and Drug Administration (FDA) first approved testosterone therapy in the early 1970s to treat a medical condition known as hypogonadism. [read post]
31 Oct 2015, 9:52 pm by William D. Kickham
  Largely, two reasons:  1) Prenatal screening tests are not subject to testing and approval by the Food and Drug Administration (FDA.) [read post]
29 Oct 2015, 9:10 am by Christopher Hoffmann
Food and Drug Administration recommended that physicians should consider prescribing a lower dose of sleeping pills like Ambien to many patients. [read post]
28 Oct 2015, 10:01 pm by Dan Flynn
Food and Drug Administration’s (FDA’s) Office of Criminal Investigation (OCI). [read post]
28 Oct 2015, 4:30 am
  Behold its splendor and majesty: "In a product liability action against a manufacturer or seller, a product that is a drug is not defective or unreasonably dangerous, and the manufacturer or seller is not liable, if the drug was approved for safety and efficacy by the United States food and drug administration, and the drug and its labeling were in compliance with the United States… [read post]
25 Oct 2015, 10:01 pm by Cookson Beecher
Food and Drug Administration’s (FDA) Food Safety Modernization Act (FSMA) Produce Rule is expected to be finalized and published soon. [read post]
20 Oct 2015, 3:56 pm by News Desk
“The ‎duties of the United States Marshals Service vary in scope and nature and include enforcing all federal court orders such as the one executed today with our partners from the Food and Drug Administration and the U.S. [read post]
20 Oct 2015, 3:33 pm by Drew Falkenstein
” “The ‎duties of the United States Marshals Service vary in scope and nature and include enforcing all federal court orders such as the one executed today with our partners from the Food and Drug Administration and the U.S. [read post]
13 Oct 2015, 6:11 am by Law Offices of Jeffrey S. Glassman
The problem with these medications, including Xarelto, is that some patients will develop a serious internal bleeding disorder while taking Xaretlo, and there is no antidote currently approved by the United States Food and Drug Administration (FDA) to treat these patients. [read post]
12 Oct 2015, 9:29 am
  North Carolina has codified the learned intermediary doctrine, but its codification mentions only prescription drugs, not medical devices: [N]o manufacturer or seller of a prescription drug shall be liable in a products liability action for failing to provide a warning or instruction directly to a consumer if an adequate warning or instruction has been provided to the physician or other legally authorized person who prescribes or dispenses that prescription drug for… [read post]
12 Oct 2015, 7:15 am by Hardee Bass
Food and Drug Administration, the FDA, took the unprecedented step of issuing a warning letter to SFNTC for violations of the 2009 Family Smoking Prevention and Control Act due to some of the claims that it is making about the American Spirit cigarette. [read post]