Use of Advisory Committees by the Food and Drug Administration: Hearings Before a Subcommittee of the Committee on Government Operations, House of Representatives, Ninety-third Congress, Second Session ...U.S. Government Printing Office, 1976 |
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Стр. 3
... health - related claims on food labels . Since 1984 , the Food and Drug Administration has been taking a close look at its longstanding policy discouraging health claims on food labels . This review resulted in FDA's August 4 , 1987 ...
... health - related claims on food labels . Since 1984 , the Food and Drug Administration has been taking a close look at its longstanding policy discouraging health claims on food labels . This review resulted in FDA's August 4 , 1987 ...
Стр. 15
... health and disease - related claims on food labeling . The Agency has taken the position that there are basically two ways , which are not mutually exclusive , in which health - related labeling claims can cause a food to violate the ...
... health and disease - related claims on food labeling . The Agency has taken the position that there are basically two ways , which are not mutually exclusive , in which health - related labeling claims can cause a food to violate the ...
Стр. 22
... health - related information . attempts to make fraudulent claims as there have been in the past , and these attempts must be overcome with strong regulatory actions . However , we also know that there may be I would like to take the ...
... health - related information . attempts to make fraudulent claims as there have been in the past , and these attempts must be overcome with strong regulatory actions . However , we also know that there may be I would like to take the ...
Стр. 24
... health - related claims on food labels without prior approval , but as our proposal points out , this entails some risk , in that if a manufacturer fails to adhere to the criteria , the product and the manufacturer's activity may be ...
... health - related claims on food labels without prior approval , but as our proposal points out , this entails some risk , in that if a manufacturer fails to adhere to the criteria , the product and the manufacturer's activity may be ...
Стр. 35
... health - related claims represent a new approach in how FDA plans to regulate food labeling and , quite frankly , because the agency needs some experience in applying the criteria in order to determine whether they are in fact workable ...
... health - related claims represent a new approach in how FDA plans to regulate food labeling and , quite frankly , because the agency needs some experience in applying the criteria in order to determine whether they are in fact workable ...
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adequate advertising agency All-Bran American Dental Association American Endodontic Society appropriate cancer CFSAN Chairman cholesterol claims on food clinical Commissioner concerning CONGRESS THE LIBRARY consensus consumers Cosmetic Act criteria Dental Association dentistry develop diet and health dietary fiber dietary supplements discuss disease document draft Drug Administration endodontists evaluate FDA's Federal Food Federal Register fiber Food and Drug food labeling food products FOUNTAIN Glick gutta percha health claims health-related claims health-related information information on food ingredients intake issue Kellogg Kellogg Company letter to dentist LIBRARY OF CONGRESS manufacturers material memo memorandum messages on food misbranded misleading nutrients nutrition nutrition labeling prevention proposed rule public health messages RC2B recommended referred regulations relationship between diet requirements root canal root canal therapy Sargenti Method saturated fat scientific evidence statement subcommittee substantial technique therapeutic tion total dietary pattern treatment vitamins WEISS WERTS YOUNG
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Стр. 4 - Mr. Chairman, and members of the subcommittee, I wish to thank you for the opportunity to appear before you today in support of planning funds for the Eau Galle River flood control project.
Стр. 21 - Secretary's approval, the regulation is then forwarded to the Office of Information and Regulatory Affairs in the Office of Management and Budget (OMB) for review under Executive Order 12291.
Стр. 302 - drug," as used in this Act, shall include all medicines and preparations recognized in the United States Pharmacopoeia or National Formulary for internal or external use, and any substance or mixture of substances intended to be used for the cure, mitigation, or prevention of disease of either man or other animals. The term
Стр. 305 - Any drug (except a new animal drug or an animal feed bearing or containing a new animal drug) the composition of which is such that such drug, as a result of investigations to determine its safety and effectiveness for use under such conditions, has become so recognized, but which has not, otherwise than in such investigations, been used to a material extent or for a material time under such conditions.
Стр. 304 - ... no person shall introduce or deliver for introduc-tion into interstate commerce any...
Стр. 298 - Formulary, or any supplement to any of them ; and (2) articles intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or other animals; and (3) articles (other than food) intended to affect the structure or any function of the body of man or other animals...
Стр. 298 - drug" means (1) articles recognized in the official United States Pharmacopoeia, official Homeopathic Pharmacopoeia of the United States, or official National Formulary, or any supplement to any of them ; and (2) articles intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or other animals; and...
Стр. 298 - ... articles (other than food) intended to affect the structure or any function of the body of man or other animals; and (D) articles intended for use as a component of any articles specified in clause (A), (B), or (C); but does not include devices or their components, parts, or accessories.
Стр. 304 - new drug" means — (1) Any drug the composition of which is such that such drug is not generally recognized, among experts qualified by scientific training and experience to evaluate the safety of drugs, as safe for use under the conditions prescribed, recommended, or suggested in the labeling thereof, except that such a drug not so recognized shall not be deemed to be a "new drug...
Стр. 407 - Commissioner Food and Drug Administration 5600 Fishers Lane Rockville, Maryland 20857 Dear Dr.