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15 Feb 2016, 8:10 am
Food and Drug Administration to have the same effectiveness and bioequivalent range. [read post]
5 Feb 2009, 4:36 am
Senate Bill 101 would grant new protections from product-liability suits to Georgia companies whose products have Food and Drug Administration approval. [read post]
25 Aug 2014, 6:54 pm
Food & Drug Administration and the U.S. [read post]
20 May 2015, 11:10 am
Food and Drug Administration (FDA) is warning that the type 2 diabetes medicines [Invokana (canagliflozin), Farxiga (dapagliflozin), and Jardiance (empagliflozin)] may lead to ketoacidosis, a serious condition where the body produces high levels of blood acids called ketones that may require hospitalization. [read post]
29 Mar 2023, 9:05 pm
Investigators with the Food and Drug Administration have not yet determined what food or beverage is the source of the Salmonella. [read post]
14 Oct 2021, 9:03 pm
Food and Drug Administration’s public health mission is to reduce the burden of chronic disease through improved nutrition. [read post]
9 Nov 2019, 9:03 pm
The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
27 Apr 2010, 3:50 am
The New York Times reports the Food and Drug Administration plans to "tighten their oversight" of medical devices, including infusion pumps that automatically deliver drugs and food to hospital patients. [read post]
19 Jun 2012, 8:55 am
Almost immediately after Propecia was approved by the Food and Drug Administration in 1997, a number of doctors and researchers began expressing their concerns about the potential side effects of the hair loss drug. [read post]
26 Aug 2012, 3:34 pm
Food and Drug Administration (FDA) approved safety labeling changes to packaging for Propecia, a very well-known drug taken by men for hair loss. [read post]
Expansion to FTC’s Orange Book Campaign Leads to Calls for More Clarity from Pharmaceutical Industry
1 May 2024, 9:15 am
Food & Drug Administration’s (FDA) Orange Book. [read post]
23 Aug 2019, 7:18 am
Food and Drug Administration (FDA) announced in the Federal Register that a proposed collection of information on the Review Transparency and Communication in Reviews of 351(k) Biologics License Applications in Biosimilars User Fee Act has been submitted to the Office of Management and Budget (OMB) for review and approval. [read post]
1 Mar 2013, 9:00 am
Food and Drug Administration Could Tighten Controls on Hydrocodone Combination Drugs.... [read post]
1 Feb 2016, 9:00 am
., Board Certified by The Florida Bar in Health Law In May of 2015, Tricare began screening all compound medication prescriptions to ensure approval of each ingredient with the Food and Drug Administration (FDA). [read post]
22 Jan 2014, 9:01 am
On January 13, 2014, the Food and Drug Administration issued a draft guidance document entitled "Fulfilling Regulatory Requirements for Postmarketing Submissions of Interactive Promotional Media for Prescription Human and Animal Drugs and Biologics." [read post]
27 Feb 2012, 9:16 pm
Food and Drug Administration recently published its long-awaited guidance documents on Biosimilars/Biosimilarity (see "FDA Publishes Draft Guidelines for Biosimilar Product Development" and "More on FDA Draft Guidelines for "Follow-on" Biologic Drug Approval Pathway"). [read post]
1 Feb 2016, 9:00 am
., Board Certified by The Florida Bar in Health Law In May of 2015, Tricare began screening all compound medication prescriptions to ensure approval of each ingredient with the Food and Drug Administration (FDA). [read post]
17 Feb 2016, 9:00 am
., Board Certified by The Florida Bar in Health Law In May of 2015, Tricare began screening all compound medication prescriptions to ensure approval of each ingredient with the Food and Drug Administration (FDA). [read post]
29 Nov 2012, 1:59 pm
Food and Drug Administration approved NextWave's drug Quillivant XR in September. [read post]
1 Mar 2013, 9:00 am
Food and Drug Administration Could Tighten Controls on Hydrocodone Combination Drugs.... [read post]
