14,474 results found

Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments and Listing of Ingredients in Tobacco Products.

Dietary Supplement Labeling Requirements and Recommendations Under the Dietary Supplement and Nonprescription Drug Consumer Protection Act...

In the August 25, 2014, Federal Register, FDA announced the renewal of certain FDA advisory committees for an additional two years beyond the charter expiration date.

In the May 18, 2015, Federal Register, FDA announced the availability of grant funds for the support of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use.

Various testing measures and labeling will be required to mitigate the identified risks of adverse tissue reaction, ineffective marking, and improper use.

In the July 2, 2015, Federal Register, FDA announced the selection of disease areas to be addressed during fiscal years 2016–2017 of its Patient-Focused Drug Development Initiative.

On December 5, 2024, FDA unveiled the draft guidance for industry regarding accelerated approval for drugs and biologics.

The draft guidance will provide questions and answers on topics related to compliance, labeling of added sugars, declaration of quantitative amounts of vitamins and minerals, and format for Nutrition and Supplement Facts labels.

FDA issued a notice establishing the rare pediatric disease priority review fee rate for FY2015 at $2,562,000 and outlining FDA's procedures for payment.

FDA announced it has filed with the Library of Congress the annual reports of those FDA advisory committees that held closed meetings during fiscal year 2014.

FDA announced its filing of a citizen petition proposing the color additive regulations be amended to provide for the safe use of spirulina extract as a color additive.

FDA announced its filing of a citizen petition, proposing that the food additive regulations be amended to provide for the safe use of ionizing radiation to treat mesquite bean flour.

In the May 30, 2017, Federal Register, FDA announced that BASF Corporation filed a petition on February 10, 2017, proposing that the food additive regulations...

In the November 24, 2015, Federal Register, FDA announced that BASF Corp. filed a petition on October 15, 2015.

Authorized by the Food Safety Modernization Act, these fees are effective October 1, 2014, through September 30, 2015.

The FDA announced an opportunity for a hearing on a proposal to revoke the biologics license issued to Allergy Laboratories, Inc.

The FDA called for comments to a food additive petition by DSM Nutritional Products proposing the safe use of 25-hydroxyvitamin D3 in feed for turkeys.

In the April 22, 2015, Federal Register, FDA announced a petition to amend color additive regulations...