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16 Jul 2021, 9:52 pm
The Food and Drug Administration (“FDA”) and U.S. [read post]
15 Jul 2021, 6:43 pm
The United States has been supportive but distant from the development of what is emerging as a consensus position on the expectations of business (and their supply chains) in the context of human rights effects of their economic activities. [read post]
13 Jul 2021, 4:05 pm
and 7 U.S.C. 2321 et seq.), in consultation with the Under Secretary of Commerce for Intellectual Property and Director of the United States Patent and Trademark Office, submit a report to the Chair of the White House Competition Council, enumerating and describing any relevant concerns of the Department of Agriculture and strategies for addressing those concerns across intellectual property, antitrust, and other relevant laws. [read post]
13 Jul 2021, 4:05 pm
and 7 U.S.C. 2321 et seq.), in consultation with the Under Secretary of Commerce for Intellectual Property and Director of the United States Patent and Trademark Office, submit a report to the Chair of the White House Competition Council, enumerating and describing any relevant concerns of the Department of Agriculture and strategies for addressing those concerns across intellectual property, antitrust, and other relevant laws. [read post]
12 Jul 2021, 8:02 am
In 2020, the Food and Drug Administration (FDA) issued a recall of all packages of Zantac and ranitidine products from all stores and distributors across the United States. [read post]
12 Jul 2021, 8:02 am
In 2020, the Food and Drug Administration (FDA) issued a recall of all packages of Zantac and ranitidine products from all stores and distributors across the United States. [read post]
12 Jul 2021, 8:02 am
In 2020, the Food and Drug Administration (FDA) issued a recall of all packages of Zantac and ranitidine products from all stores and distributors across the United States. [read post]
11 Jul 2021, 9:05 pm
For example, the association stated that sanitizing hand-held knives between each carcass is not reasonable, nor would it result in significant pathogen reduction on final products. [read post]
9 Jul 2021, 2:00 am
This is based on both concerns that the vaccines have not yet been fully approved by the Food and Drug Administration (FDA) and the uncertain legal environment that still exists and “the long list of legal considerations the E.E.O.C. says they must follow before mandating vaccines. [read post]
8 Jul 2021, 9:03 pm
Food and Drug Administration (FDA) updated the prescription label to Aduhelm, a recently released Alzheimer’s drug, to limit its recommended use to patients with mild Alzheimer’s or mental impairment. [read post]
8 Jul 2021, 6:14 am
Device malfunctions reported to the United States Food and Drug Administration (FDA) are typically available to the public in the MAUDE database, which stands for Manufacturer and User Facility Device Experience. [read post]
8 Jul 2021, 6:14 am
Device malfunctions reported to the United States Food and Drug Administration (FDA) are typically available to the public in the MAUDE database, which stands for Manufacturer and User Facility Device Experience. [read post]
8 Jul 2021, 6:14 am
Device malfunctions reported to the United States Food and Drug Administration (FDA) are typically available to the public in the MAUDE database, which stands for Manufacturer and User Facility Device Experience. [read post]
5 Jul 2021, 9:03 pm
Food and Drug Administration (FDA) approved aducanumab, a therapy for the treatment of Alzheimer’s disease sponsored by Biogen, which will be commercialized under the brand name Aduhelm. [read post]
1 Jul 2021, 9:05 pm
The Food and Drug Administration unveiled the plan yesterday, July 1, referencing the first known contamination in U.S. produce in 2018, as well as an outbreak that year traced to McDonald’s salads. [read post]
30 Jun 2021, 5:27 am
The United States Food and Drug Administration (FDA) sets the daily allowable limit of NDMA for humans at 96 nanograms. [read post]
30 Jun 2021, 5:27 am
The United States Food and Drug Administration (FDA) sets the daily allowable limit of NDMA for humans at 96 nanograms. [read post]
30 Jun 2021, 5:27 am
The United States Food and Drug Administration (FDA) sets the daily allowable limit of NDMA for humans at 96 nanograms. [read post]
29 Jun 2021, 9:05 pm
Food and Drug Administration’s (FDA) call for convalescent plasma—blood collected from individuals who have recovered from COVID-19—brought attention to these policies that prohibit some men from donating plasma under FDA’s policy on donations from men who have sex with men (MSM). [read post]
29 Jun 2021, 2:02 pm
District Court Judge Lynn Hughes the court upheld the Hospital’s mandatory vaccination policy that carved out narrow exceptions to employee-inoculation by any of the three vaccinations authorized on an emergency use basis by the United States Food and Drug Administration (“FDA”) based upon medical conditions or sincerely held religious beliefs. [read post]
