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5 Aug 2022, 1:56 pm by Patrick A. Malone
The ink was barely dry on statements from the head of the federal Food and Drug Administration about a planned external, independent review of the agency’s tobacco oversight division when one of its top regulators created a personnel stink of his own. [read post]
25 May 2012, 11:37 am by Walter Olson
Amish raw-milk farmers beware: as Mike Riggs reports at Reason, Senator Rand Paul of Kentucky introduced an amendment that would have curtailed the power of Food and Drug Administration agents to carry firearms and make warrantless arrests — the agency would still have retained many other legal weapons with which to secure compliance with its will — but the amendment failed by a 78-15 vote. [read post]
28 Feb 2011, 9:34 am
Food & Drug Administration (FDA) recently acknowledged the risk of zinc poisoning associated with denture cream usage. [read post]
20 May 2012, 9:16 pm by Patent Docs
Food and Drug Administration held a public hearing on the Draft Guidance on Biosimilar Development, where researchers, payors, patient and physician groups, and industry advocates provided their thoughts on the FDA's first attempt to clarify the logistics as to the operation of the Biologics Price Competition and Innovation Act of 2009 (BPCIA). [read post]
27 May 2010, 4:09 pm by Larry Jones
The federal Food & Drug Administration is notifying patients that it has approved a revised label for Xenical to include new safety information about cases of severe liver injury that have been reported rarely with the use of this medication. [read post]
30 Jan 2012, 1:29 pm by Doug Isenberg
The Food and Drug Administration secretly monitored the personal e-mail of a group of its own scientists and doctors after they warned Congress that the agency was approving medical devices that they believed posed unacceptable risks to patients, government documents show. [read post]
16 Dec 2010, 7:00 am by Kim Wood
The Food and Drug Administration is cracking down on manufacturers of certain weight loss, body building and sexual enhancement supplements that contain potentially dangerous ingredients. [read post]
14 Jul 2020, 6:51 am by Robert Kraft
The Washington Times reports the Food and Drug Administration on Thursday “approved a test to detect and differentiate viruses that cause flu and COVID-19 in people suspected of having the coronavirus. [read post]
21 Sep 2019, 8:08 am by Throneberry Law Group
According to the Food and Drug Administration (FDA), consumers are advised to immediately cease using four products produced by Beauty Plus Global Inc after testing  by the FDA revealed those items showed asbestos contamination. [read post]
28 Feb 2011, 9:55 pm by Patent Docs
Food and Drug Administration (FDA). [read post]
7 Jan 2011, 8:16 am
The Food and Drug Administration (FDA) was granted regulatory power over tobacco companies in 2009. [read post]
26 Mar 2012, 4:11 pm
Food and Drug Administration released the findings of an investigation at Jensen Farms. [read post]
4 Oct 2016, 3:11 am by Bob Kraft
Louis Post-Dispatch reports that the Food and Drug Administration “has reclassified surgical mesh used to repair pelvic organ prolapse as ‘high risk,’ citing thousands of reports of complications involving its use. [read post]
20 Nov 2014, 1:45 pm by Bill Marler
The Massachusetts Department of Health confirmed on Thursday afternoon that the agency, along with the Centers for Disease Control and Food and Drug Administration, are investigating a potential multi-state salmonella cluster. [read post]
21 Jun 2012, 2:49 pm
The implicated sprouts are in 6-ounce, clear plastic containers with a Universal Product Code of 75465-55912, according to the recall notice posted by the Food and Drug Administration on June 21. [read post]
29 Sep 2010, 9:59 pm by Patent Docs
By Donald Zuhn -- Last week, the congressional daily The Hill reported on a draft notice from the Food and Drug Administration (FDA) that was being circulated among healthcare lobbyists on Capitol Hill. [read post]
23 Apr 2012, 9:59 pm by Patent Docs
Food and Drug Administration on April 2, Abbott Laboratories requested that the FDA refrain from accepting biosimilar applications under the Biologics Price Competition and Innovation Act (BPCIA) that cite reference products (biologics) for which a biologics license application (BLA) was submitted to the FDA prior to March 23, 2010. [read post]
29 Jun 2012, 7:58 am
" According to the AP, "the Food and Drug Administration asked its 18-member panel to recommend guidelines for monitoring more than a half-million US patients with metal hip replacements. [read post]
1 Jul 2016, 6:18 am by Patrick A. Malone
The Food and Drug Administration has approved the preliminary testing  of GLS-5700, an experimental vaccine by Inovio, of Plymouth Meeting, Pa., and GeneOne Life Science, of Seoul, South Korea. [read post]