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. 2
... ingredients : paraformalde- hyde , lead oxide , hydrocortisone and / or prednisolone . One of the things we want to find out in this hearing is whether drugs of this type have been demonstrated to be safe and effective . They may be ...
... ingredients : paraformalde- hyde , lead oxide , hydrocortisone and / or prednisolone . One of the things we want to find out in this hearing is whether drugs of this type have been demonstrated to be safe and effective . They may be ...
Стр. 4
... ingredient in N2— is contraindicated in endodontic therapy . Drugs are considered merely adjunctive to proper debridement , bactericidal irrigation , and dimen- sional filling of the root canal . The least irritating drug should be ...
... ingredient in N2— is contraindicated in endodontic therapy . Drugs are considered merely adjunctive to proper debridement , bactericidal irrigation , and dimen- sional filling of the root canal . The least irritating drug should be ...
Стр. 12
... ingredients tend to vary from batch to batch . This information was developed and has been attested to by both the Food and Drug Administration of the United States of America and by the Commonwealth Bureau of Dental Standards of ...
... ingredients tend to vary from batch to batch . This information was developed and has been attested to by both the Food and Drug Administration of the United States of America and by the Commonwealth Bureau of Dental Standards of ...
Стр. 17
... ingredients were added to the material . For example , a mercurial compound appeared and corticosteroids , reduced in percentage , were broken up in two types , prednisolone and hydrocortisone . The lead tetroxide was reduced in ...
... ingredients were added to the material . For example , a mercurial compound appeared and corticosteroids , reduced in percentage , were broken up in two types , prednisolone and hydrocortisone . The lead tetroxide was reduced in ...
Стр. 18
... ingredients were added , additives were removed , but the common denominator that we are beginning to pick up here ... ingredients , the quality of ingredients , the number of ingredients , without influencing the effec- tiveness of the ...
... ingredients were added , additives were removed , but the common denominator that we are beginning to pick up here ... ingredients , the quality of ingredients , the number of ingredients , without influencing the effec- tiveness of the ...
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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.