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30 Apr 2023, 8:00 pm
With that background, let’s get back to S. 1067, which first reared its head in Spring 2022 as an amendment to S.4348, the “Food and Drug Administration Safety and Landmark Advancements Act of 2022” (Section 511). [read post]
14 Dec 2014, 11:07 am
Also benefiting directly and indirectly from the Ebola scare, along with concerns about other infectious diseases, are the Center for Disease Control (CDC) and the Food and Drug Administration (FDA). [read post]
11 Mar 2021, 9:03 pm
Mayorkas stated that the United States would step “forward to support eligible Venezuelan nationals already present here, while their home country” combats widespread food insecurity and violence from armed groups. [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]
31 Oct 2017, 5:33 am
Many EpiPens were recalled in March of this year due to defective auto-injectors, but the United States Food and Drug Administration (FDA) has issued a warning letter stating that the manufacturer Meridian Medical Technologies failed to properly investigate reports of defective EpiPens. [read post]
3 Feb 2016, 10:50 am
Food and Drug Administration (FDA) in 2012 ordered J&J, Boston Scientific, Bard and others to report rates of organ damage and complications linked to the implants. [read post]
9 Sep 2011, 6:47 am
We are offering free case evaluations to the general public across the United States and Canada. [read post]
25 Oct 2016, 8:52 am
Food & Drug Administration (FDA) received hundreds of adverse reports about the retrievable filters. [read post]
23 Sep 2011, 1:38 pm
We are offering free case evaluations to the general public across the United States and Canada. [read post]
25 Oct 2016, 8:49 am
Food & Drug Administration (FDA) received hundreds of adverse reports about the retrievable filters. [read post]
27 Jul 2012, 1:21 am
” Cytori claims that FDA’s refusal to clear the devices for distribution in the United States is thus arbitrary and capricious. [read post]
27 Aug 2011, 2:29 pm
FDA Sets Meeting The US Food and Drug Administration (FDA) will convene a meeting of the Obstetrics-Gynecology Devices Panel of the Medical Devices Advisory Committee on September 8-9, 2011. [read post]
21 Jul 2011, 11:08 am
We are offering free case evaluations to the general public across the United States and Canada. [read post]
23 Feb 2015, 9:30 pm
In response, the White House is directing the United States Food and Drug Administration (FDA) to “develop a new approach” for regulating the sequencing technologies used to gather genetic data from patients. [read post]
14 Sep 2011, 7:55 am
We are offering free case evaluations to the general public across the United States and Canada. [read post]
6 Mar 2008, 12:39 am
OR STATE GOVERNMENT WORKS [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]
11 Mar 2020, 2:50 pm
The Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA) have long stated that the most common reason for norovirus is contaminated food or water. [read post]
14 Aug 2019, 8:17 am
Click on the image to enlarge it.But, the Food and Drug Administration “sampling assignment” that was associated with the 2018 outbreak that killed five people and sickened at least 210 across 27 states did not focus on processing facilities. [read post]
