Search for: "FOOD AND DRUG ADMINISTRATION" Results 5281 - 5300 of 23,787
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23 Apr 2020, 12:28 pm by Seyfarth Shaw LLP
Food and Drug Administration, the CDC, or other public health authorities about what tests may be considered safe and accurate. [read post]
23 Apr 2020, 7:18 am by Dennis Crouch
(Admittedly, it is not always possible to keep the invention secret, especially if regulatory approval is necessary as in the case of Food and Drug Administration’s approval to market drugs or medical devices. [read post]
22 Apr 2020, 9:04 pm by News Desk
The Food and Drug Administration’s investigation of an outbreak of E. coli 0103 in clover sprouts has been completed, and the Centers for Disease Control and Prevention has declared that the outbreak is over. [read post]
22 Apr 2020, 8:17 pm by Bill Marler
” “The FDA will hold food companies accountable when they endanger the public’s health by purveying adulterated food that causes outbreaks of illness,” said Food and Drug Administration Commissioner Stephen M. [read post]
. $22 million is allocated to the Food and Drug Administration to support testing activities, including diagnostic, serological and antigen testing, as well as related administrative functions. $600 million is provided to the Health Resources and Services Administration – Primary Health Care for grants under the Health Centers program and for grants to federally qualified health centers. $225 million is allotted to rural health clinics through… [read post]
22 Apr 2020, 9:46 am by Lawrence B. Ebert
The case concerns Tecfidera, a drug used to treat multiple sclerosis [MS]:Biogen holds the New Drug Application (“NDA”) for theactive ingredient dimethyl fumarate (“DMF”), which wasapproved by the Food and Drug Administration (“FDA”) in2013 as Tecfidera®, a twice-daily pill indicated “for thetreatment of patients with relapsing forms of multiple sclerosis” at a daily dose of 480 mg. [read post]
22 Apr 2020, 9:00 am by Staff
Questions and answers by the Food and Drug Administration regarding the regulation of CBD products for medical uses, for drug uses, use as dietary supplements, and for other uses. [read post]
21 Apr 2020, 9:10 pm by Marissa Fritz
Food and Drug Administration (FDA) approved the first generic version of the drug—thanks to the agency’s new Drug Competition Action Plan (DCAP). [read post]
21 Apr 2020, 9:05 pm by News Desk
” The fine agreement is also being touted as an example to other food companies that the Justice Department and the Food and Drug Administration are serious about enforcing food safety laws. [read post]
21 Apr 2020, 1:09 pm by Herrman & Herrman, P.L.L.C.
The Food and Drug Administration (FDA) posts daily announcements of actions it has taken in response to the COVID-19 pandemic. [read post]
21 Apr 2020, 11:07 am by Silver Law Group
Food and Drug Administration (FDA) filings and health officials, reported that Aytu was distributing unreliable COVID-19 tests from unapproved Chinese manufacturers. [read post]
21 Apr 2020, 9:31 am by Jason Gordon and Erika Auger
Food and Drug Administration (“FDA”), there currently are no products that are scientifically proven to treat or prevent the virus. [read post]
21 Apr 2020, 9:31 am by Jason Gordon and Erika Auger
Food and Drug Administration (“FDA”), there currently are no products that are scientifically proven to treat or prevent the virus. [read post]
21 Apr 2020, 6:28 am by Robert Kraft
Food and Drug Administration “modified its stance on COVID-19 and vaping, saying it has an unknown effect on the risk” of the disease, “while warning that smoking can create worse outcomes. [read post]
20 Apr 2020, 9:05 pm by Thomas Perroud
The government strictly defined admissible justifications for leaving home: food or pharmaceutical purchases, medical consultations, and imperative professional reasons. [read post]
20 Apr 2020, 4:38 pm by Jonathan Aronie and Keeley A. McCarty
To qualify as a personal respiratory protective device, however, face masks had to meet three criteria: (1) be previously approved by NIOSH, (2) be the subject of an Emergency Use Authorization (“EUA”) by the Food and Drug Administration (“FDA”), and (3) be used during and for the COVID-19 pandemic response. [read post]
20 Apr 2020, 5:01 am by Schachtman
” As would-be studies that lack probativeness for causality, they are thus ideal tools for the lawsuit industry to support litigation campaigns against drugs and medical devices. [read post]
19 Apr 2020, 9:05 pm by Cary Coglianese
Food and Drug Administration (FDA) regulatory authority over medical devices used for diagnostic testing. [read post]