Search for: "FOOD AND DRUG ADMINISTRATION" Results 481 - 500 of 23,707
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16 Apr 2013, 10:12 am by Jack McNeill
From the summary: “Over the past 10 years, 278 new drugs have been approved by the Food and Drug Administration, according to data from the InnoThink Center for Research in Biomedical Innovation. [read post]
27 Mar 2012, 2:02 pm by McNabb Associates, P.C.
FROMMER Associated Press WASHINGTON (AP) — A federal judge on Tuesday blocked the importation of a drug used in executions on grounds the Food and Drug Administration ignored the law in allowing it into this country. [read post]
21 Feb 2023, 9:00 pm by News Desk
The Food and Drug Administration is continuing its use of import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
23 Jan 2023, 9:01 pm by News Desk
The Food and Drug Administration is continuing its use of import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
13 Nov 2023, 9:00 pm by News Desk
The Food and Drug Administration continues using import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
12 Jan 2024, 9:03 pm by News Desk
The Food and Drug Administration continues using import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
15 Sep 2011, 12:00 am by Joel Outten
Public Citizen, a consumer rights advocacy group, filed a petition last month asking the US Food and Drug Administration (FDA) to amend regulations that prevent generic drug manufacturers from updating product labels with pertinent safety data.According to the petition, manufacturers of generic drugs are not authorized to update their labels through the prior-approval-supplement (PAS) or changes being-effected (CBE) procedures available to the… [read post]
15 Sep 2011, 12:00 am by Joel Outten
Public Citizen, a consumer rights advocacy group, filed a petition last month asking the US Food and Drug Administration (FDA) to amend regulations that prevent generic drug manufacturers from updating product labels with pertinent safety data.According to the petition, manufacturers of generic drugs are not authorized to update their labels through the prior-approval-supplement (PAS) or changes being-effected (CBE) procedures available to the… [read post]
7 Feb 2007, 7:59 pm
In a January 30 press release the Food and Drug Administration announced a report outlining a comprehensive commitment to the safety of drugs and other medical products. [read post]
21 Dec 2023, 4:16 pm by Sara Hinkle
The Food and Drug Administration (“FDA”) has adopted a Final Rule requiring that when a direct-to-consumer TV or radio ad for a prescription drug makes statements relating to side effects of the drug, those statements must be presented in a “clear, conspicuous, and neutral manner. [read post]
6 Jul 2022, 9:03 pm by News Desk
Food and Drug Administration on Wednesday finalized Guidance for Industry (GFI) #245: Hazard Analysis and Risk-Based Preventive Controls for Food for Animals to help animal food facilities subject to the FDA Food Safety Modernization Act (FSMA) Hazard Analysis and Risk-Based Preventive Controls for animal food requirements develop a food safety plan to prevent or significantly minimize hazards that could… [read post]
3 Oct 2022, 9:04 pm by News Desk
Food and Drug Administration is taking action to help prevent outbreaks of foodborne illnesses through the development of food safety prevention strategies for bulb onions and imported mushrooms. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
5 Aug 2022, 6:03 am by Robert Kraft
NPR reports, “A special Food and Drug Administration process to get patients earlier access to new drugs has come under fire. [read post]
31 Jan 2023, 12:03 pm by Tracey T. Gonzalez
The Food and Drug Administration (FDA) recently issued both draft and final guidance regarding food allergen labeling requirements. [read post]