Summary prepared by the Food and Drug Administration regarding the rule on children and tobacco which is aimed at regulating commercial speech to ensure that an illegal activity is not promoted.
Industry guide prepared by the Food and Drug Administration on consultation procedures regarding foods derived from new plant varieties.
Publication from the Food and Drug Administration which describes small business food labeling exemptions under 21 CFR 101.9(j)(1).
You don't need to make this decision on your own. Always consult your physician, particularly your obstetrician, be.
The landscape of laws, regulations and codes governing advertising and marketing is complex and multijurisdictional. This past year has brought about significant change for advertisers and marketers in the following areas.
Publication from the Food and Drug Administration (FDA) which explains the three classes of recalls and discusses FDA's role in the recall process.
Summary prepared by the Food and Drug Administration of the Dietary Supplement Health and Education Act.
Guide from the Food and Drug Administration which provides assistance to manufacturers of food packaging in evaluating processes for producing packaging from post-consumer recycled plastic.
Publication from the Food and Drug Administration (FDA) which explains the FDA's new food labeling regulations.
Guide from the Food and Drug Administration which explains for small businesses the legal requirements set forth in the current regulation for the labeling of juice products that have not been processed to prevent, reduce, or eliminate harmful bacteria
Backgrounder from the Food and Drug Administration which describes the Modernization Act of 1997.
Statement from the Federal Trade Commission (FTC) which provides guidance interpreting the FTC's enforcement policy with respect to the use of nutrient content and health claims in food advertising.
Question and answer guide for manufacturers engaged in exporting Food and Drug Administration regulated food and cosmetic products to a foreign country.
Industry guide prepared by the Food and Drug Administration regarding regulatory requirements for marketing cosmetics in the United States.
Publication from the Food and Drug Administration which explains the regulation of food additives under the Federal Food, Drug, and Cosmetic Act of 1938.
Manufacturers of medical devices suffered a major setback recently when a federal appellate court held that "premar.
This article concerns the newly proposed legislation facing our lawmakers in the U.S. Congress that will directly i.
Guide for consumers from the Food and Drug Administration on how to read cosmetic labels. Also describes how cosmetic labels are regulated.
Synopsis from the Food and Drug Administration for consumers regarding the principal requirements of food law.
Industry guide from the Food and Drug Administration regarding cosmetic good manufacturing.
On March17th the Food and Drug Administration (FDA) issued, amidst great fanfare, a regulation governing labels fo.
Analysis for consumers of the New Requirements for Dietary Supplement Labels from the Food and Drug Administration.
Summary from the Food and Drug Administration (FDA) of the Greensboro, North Carolina, Federal District Court's ruling on April 25, 1997 that the FDA has jurisdiction under the Federal Food, Drug, and Cosmetic Act to regulate nicotine-containing cigarettes and smokeless tobacco.
Fact sheet from the Food and Drug Administration which explains the Clinton Administration's plan to strengthen and improve food safety under the Food Safety Initiative.
Publication from the Food and Drug Administration which explains the regulation of food coloring under the Federal Food, Drug, and Cosmetic Act of 1938.