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7 Aug 2023, 10:42 am
In response, Food and Drug Administration Commissioner Robert Califf […] The post How to stop kids from vaping first appeared on Maryland Daily Record. [read post]
11 Feb 2023, 7:13 pm
Confirmed speakers include Julia Tierney (Chief of Staff, Food and Drug Administration), Anne Gussow (Supervisory Patent Examiner,... [read post]
6 Oct 2023, 7:46 am
Food and Drug Administration (FDA), and the U.S. [read post]
9 Apr 2024, 2:22 pm
Food and Drug Administration (FDA) announced on April 5, 2024, the results of its 2023 sampling assignment, testing talc-containing cosmetic products for the presence of asbestos. [read post]
17 Mar 2023, 10:05 am
Patent and Trademark Office updates Patent Term Extension listings to add Food and Drug Administration and Department of Agriculture information following collaboration initiatives; the U.S. [read post]
8 Dec 2017, 4:19 pm
A major recall has been issued by the Food and Drug Administration (FDA) that parents may be interested in, especially those with babies. [read post]
22 Jul 2015, 11:51 am
The Food and Drug Administration (FDA) has issued a serious warning regarding the use of a medical device during laparoscopic (minimally invasive) surgeries. [read post]
29 Mar 2024, 5:52 am
Food and Drug Administration (FDA), and the U.S. [read post]
6 Mar 2013, 9:59 pm
Food and Drug Administration, asking the agency to 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 (see "Abbott Asks FDA to Refuse Certain Biosimilar Applications"). [read post]
14 Apr 2016, 9:27 pm
Food and Drug Administration approved Celltrion's application to market Inflectra, a biosimilar to Janssen Biotech Inc.'s REMICADE (infliximab) anti-TNF-α antibody. [read post]
28 Jan 2015, 4:15 am
.; Continuum Health Management, LLC; and Mountain States Health Properties, LLC to provide their employees with health coverage for “[a]ll Food and Drug Administration approved contraceptive methods, sterilization procedures, and patient education and counseling for all women with reproductive capacity,” ...to which plaintiffs object on religious grounds.AP reports on the decision. [read post]
22 Jul 2015, 11:51 am
The Food and Drug Administration (FDA) has issued a serious warning regarding the use of a medical device during laparoscopic (minimally invasive) surgeries. [read post]
14 Sep 2017, 9:17 pm
Food and Drug Administration approved Amgen's application to market Mvasi (bevacizumab-awwb), a biosimilar to Genentech's Avastin therapeutic antibody for the treatment of multiple types of cancer. [read post]
30 Aug 2021, 9:15 am
Food and Drug Administration’s (FDA’s) electronic Orange Book indicating... [read post]
2 Feb 2008, 12:36 pm
Food and Drug Administration (FDA) announced on January 25, 2008, a nationwide recall of all lots of heparin and saline pre-filled flush syringes manufactured by AM2 PAT, Inc., of Angier, N.C. [read post]
6 Jun 2012, 1:39 pm
Food and Drug Administration had acted arbitrarily in citing time and resource constraints in declining to limit the use of antibiotics in animal feed. [read post]
9 May 2019, 10:00 am
Although accusations of research fraud and misconduct have been present for decades, the number of complaints is on the rise, according to the Food and Drug Administration (FDA).... [read post]
7 Nov 2021, 9:59 pm
Food and Drug Administration issued Final Guidance entitled "Questions and Answers on Biosimilar Development and the BPCI Act: Guidance for Industry," and Draft Guidance entitled "New and Revised Draft Q&As on Biosimilar Development and the BPCI Act (Revision 2). [read post]
17 Mar 2023, 10:05 am
Patent and Trademark Office updates Patent Term Extension listings to add Food and Drug Administration and Department of Agriculture information following collaboration initiatives; the U.S. [read post]
7 Jan 2022, 8:22 am
‘Paramount importance’: Judge orders FDA to hasten release of Pfizer vaccine docsBy Jenna Greene, Reuters, Jan. 7, 2022A federal judge in Texas on Thursday ordered the Food and Drug Administration to make public the data it relied on to license Pfizer’s COVID-19 vaccine, imposing a dramatically accelerated schedule that should result in the release of all information within about eight months.That’s roughly 75 years and four months faster than the… [read post]
