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2 Aug 2011, 2:59 am
Food and Drug Administration over drug residues in animals recently sold for slaughter as human food.De Jong received a July 6 warning letter and Valmont received a July 12 warning letter from FDA, which advised the dairies of their violations of the Federal Food, Drug, and Cosmetic Act.De Jong sold a cow for slaughter as human food last Sept. 1, which was subjected to tissue sampling by USDA's Food Safety and Inspection… [read post]
25 Aug 2009, 9:42 am
The Food and Drug Administration (FDA) has announced that it is investigating reports of liver damage in patients taking the nonprescription weight loss drug “alli. [read post]
2 Apr 2024, 9:50 am by Jonathan H. Adler
If doctors who believe the Food & Drug Administration mistakenly approved or deregulated a drug cannot sue the FDA, can anyone else? [read post]
4 Feb 2015, 9:20 pm
While the United States Food and Drug Administration (FDA) has only approved testosterone replacement therapy drugs to treat an extremely rare condition known as hypogonadism, drug companies have created a new market for their once seldom used product. [read post]
16 Nov 2009, 1:20 pm
Zambri, Esquire The New York Times reported that according to the US Food and Drug Administration (FDA), "Vials of five different Genzyme drugs for rare diseases may be contaminated with tiny particles of steel, rubber or fiber that could potentially harm patients. [read post]
9 Sep 2012, 9:36 am by Brenda Fulmer
Food and Drug Administration, charged with the responsibility of making sure they are safe and effective before they are released? [read post]
30 Jul 2024, 10:00 pm
The US Food and Drug Administration (FDA) issued final guidance titled Foods Derived from Plants Produced Using Genome Editing (Genome-Edited Plants Guidance), describing the agency’s approach for evaluating the safety of foods derived from genome-edited plant varieties. [read post]
30 Jul 2024, 10:00 pm
The US Food and Drug Administration (FDA) issued final guidance titled Foods Derived from Plants Produced Using Genome Editing (Genome-Edited Plants Guidance), describing the agency’s approach for evaluating the safety of foods derived from genome-edited plant varieties. [read post]
30 Jul 2024, 10:00 pm
The US Food and Drug Administration (FDA) issued final guidance titled Foods Derived from Plants Produced Using Genome Editing (Genome-Edited Plants Guidance), describing the agency’s approach for evaluating the safety of foods derived from genome-edited plant varieties. [read post]
30 Jul 2024, 10:00 pm
The US Food and Drug Administration (FDA) issued final guidance titled Foods Derived from Plants Produced Using Genome Editing (Genome-Edited Plants Guidance), describing the agency’s approach for evaluating the safety of foods derived from genome-edited plant varieties. [read post]
30 Jul 2024, 10:00 pm
The US Food and Drug Administration (FDA) issued final guidance titled Foods Derived from Plants Produced Using Genome Editing (Genome-Edited Plants Guidance), describing the agency’s approach for evaluating the safety of foods derived from genome-edited plant varieties. [read post]
30 Jul 2024, 10:00 pm
The US Food and Drug Administration (FDA) issued final guidance titled Foods Derived from Plants Produced Using Genome Editing (Genome-Edited Plants Guidance), describing the agency’s approach for evaluating the safety of foods derived from genome-edited plant varieties. [read post]
29 Jul 2008, 11:13 am
  Guinea pigs often receive money, accommodations, food, and other benefits to sacrifice some time for testing. [read post]
21 Jul 2020, 11:13 am by Burton A. Padove
Recently, a national outlet published a report that the Food and Drug Administration (FDA) and the U.S. [read post]
31 Mar 2009, 10:07 am
Supreme Court ruled against the drug-maker Wyeth with a 6-3 vote stating that the pharmaceutical company can be held liable for harm caused by medicines even if they carry warning labels that have been approved by the Food and Drug Administration. [read post]
10 May 2023, 9:06 pm by Dan Flynn
Taylor is the retired Food and Drug Administration Deputy Commissioner for Foods and Veterinary Medicine. [read post]
4 May 2023, 3:27 pm by Lynn L. Bergeson and Carla N. Hutton
Food and Drug Administration (FDA) announced on May 3, 2023, that it has filed a color additive petition (CAP 3C0325), submitted by the Environmental Defense Fund (EDF), the Center for Environmental Health (CEH), the Center for Food Safety (CFS), the Center for Science in the Public Interest (CSPI), and the Environmental Working Group (EWG). 88 Fed. [read post]
19 Jul 2017, 7:51 am by Robert Kraft
The Washington Post reports former Food and Drug Administration Commissioners Robert Califf, Margaret Hamburg, Andrew von Eschenbach, and Mark McClellan signed an open letter posted by the Margolis Center for Health Policy at Duke University “warning Congress that legalizing the importation of drugs from other countries – an idea that has drawn support from both Bernie Sanders and Donald Trump – is a risky approach that would endanger… [read post]
2 Mar 2007, 4:24 pm
Food and Drug Administration (FDA) today issued final guidance that describes FDA ’s current approach to communicating... [read post]