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17 Jan 2023, 4:15 am by Alec Pronk
Food & Drug Administration collaboration on Thursday; a panel discussion at the American Enterprise Institute about the near-term future for financial markets; and a discussion with IP experts at the USPTO about IP protection in China. [read post]
19 Apr 2011, 3:18 pm by Tiffany Chiao
Food and Drug Administration (FDA) announced discovery of a plot to fake certification of Chinese grains as organic. [...] [read post]
24 Mar 2016, 4:08 pm by Eric Needs
On Monday, the Food and Drug Administration said the powder added to some types of latex gloves can cause potential wound inflammation, breathing problems and scarThe post FDA is Banning Powdered Surgical Gloves appeared first on Legal Reader. [read post]
17 Jan 2022, 10:00 pm
In two draft companion guidance documents, the US Food and Drug Administration (FDA) establishes a proposed framework for transitioning medical devices currently marketed under emergency use authorization (EUA) or enforcement policy guidance to permanent marketing authorization. [read post]
25 Feb 2014, 6:51 am by AIPLA
The Court will hear oral argument as follows: on February 26, in two cases on granting (Octane Fitness) and reviewing (Highmark) attorneys’ fee awards; on March 31, in a case (Alice Corp.) on patent eligibility of system and computer-implemented method claims; on April 21, in a case (POM Wonderful) on claims under Section 43 of the Lanham Act challenging labels regulated by the Food and Drug Administration; on April 22, in a case (Aereo) on whether a provider of… [read post]
26 Oct 2023, 9:02 am by PP&S Team
More than 105,000 medical device reports were sent by the breathing machine manufacturer Phillips to the Food and Drug Administration (FDA) between April 2021 and June 2023. [read post]
2 Mar 2023, 10:00 pm
Partners Michele Buenafe, Jacob Harper, and Andrew Gray wrote the first of a two-part article series for Med Device Online, covering the existing US Food and Drug Administration (FDA) programs, recently issued guidance impacting artificial intelligence and machine learning technologies intended for use in healthcare, and what to expect from the FDA’s FY 2023 priority list. [read post]
5 May 2016, 9:38 am by William Helbling
[JURIST] The US Food and Drug Administration (FDA) on Thursday announced [press release] the finalization of a new rule that extends its regulatory power to all tobacco products, including e-cigarettes, cigars and more. [read post]
4 Jan 2024, 10:00 pm
The US Federal Trade Commission (FTC), supported by the US Food and Drug Administration (FDA), recently issued a policy statement describing how the FTC intends to “scrutinize improper Orange Book listings” to identify potential violations of Section 5 of the FTC Act, which prohibits “unfair methods of competition. [read post]
17 Apr 2023, 10:00 pm
They cover how although the Fifth Circuit recently stayed a Texas federal court's ruling that invalidated the US Food and Drug Administration's (FDA) approval of a commonly used abortion medication, several points made by the courts are worth considering for their potential effect on FDA authority and the challenges they may create for the life sciences industry. [read post]
13 Sep 2016, 6:18 pm by Andrea Tucker
On September 2, 2016, the Food and Drug Administration, FDA, enacted a final rule banning the sale of some antibacterial soaps. [read post]
17 Apr 2023, 10:00 pm
They cover how although the Fifth Circuit recently stayed a Texas federal court's ruling that invalidated the US Food and Drug Administration's (FDA) approval of a commonly used abortion medication, several points made by the courts are worth considering for their potential effect on FDA authority and the challenges they may create for the life sciences industry. [read post]
18 Mar 2021, 4:44 am by Staff
Johnson & Johnson’s adenovirus-based vaccine for preventing the transmission of COVID-19 is expected to be reviewed by the Food and Drug Administration in February 2021. [read post]
3 Dec 2020, 2:32 pm by Johanna Alonso
With Moderna and Pfizer having both requested emergency Food and Drug Administration authorization for their COVID-19 vaccine candidates, it’s only a matter of time until hospitals across the state of Maryland begin distributing them. [read post]
20 Jun 2024, 10:00 pm
Last year, the US Food and Drug Administration (FDA) announced that it would delay enforcement of certain requirements under the Modernization of Cosmetics Regulation Act (MoCRA) until July 1, 2024 to give the industry more time to comply with pending deadlines. [read post]
20 Jan 2021, 10:00 pm
Related to potential home-testing options, our FDA team has published a LawFlash on the Food and Drug Administration’s (FDA’s) Emergency Use Authorizations (EUAs) for the first over-the-counter (OTC) COVID-19 test to be performed at home, the first OTC home sample collection kit for COVID-19 testing, and additional prescription at-home tests and sample collection kits. [read post]
1 Feb 2021, 10:00 pm
Members of our vaccine taskforce recently published an important Insight outlining a selection of key legal considerations and updates as the COVID-19 vaccine rollout continues to take shape, including the status of the US Food and Drug Administration’s vaccine products, distribution, key legal issues at the state level, employer mandates and employee incentives, and important liability concerns. [read post]
23 Sep 2005, 3:57 pm
[JURIST] AP is reporting that Lester Crawford [official profile], commissioner of the Food and Drug Administration [official website], has resigned. 4:08 PM ET - Crawford's resignation comes just two months after his Senate confirmation as FDA chief [JURIST report]. [read post]