FDA Consumer, Volum 7U.S. Department of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, 1973 |
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Side 19735
... standards of quality and safety of all biological products including vaccines , has done extensive research into and regulation of flu vaccines . It has been found that influenza , one of the world's greatest respiratory disease ...
... standards of quality and safety of all biological products including vaccines , has done extensive research into and regulation of flu vaccines . It has been found that influenza , one of the world's greatest respiratory disease ...
Side 7
... standard for use of that virus . This is done by adding .5 cubic centimeter of the various dilutions to an equal amount of red blood cells from a chicken in wells of a tray . Agglutination forms a uniform haziness at the botom of the ...
... standard for use of that virus . This is done by adding .5 cubic centimeter of the various dilutions to an equal amount of red blood cells from a chicken in wells of a tray . Agglutination forms a uniform haziness at the botom of the ...
Side 11
... standard could significantly reduce a hazard , it can ban a product entirely . The impetus for development of a safety standard may come from within the Commission , from a proposal by the Product Safety Advisory Council , from a ...
... standard could significantly reduce a hazard , it can ban a product entirely . The impetus for development of a safety standard may come from within the Commission , from a proposal by the Product Safety Advisory Council , from a ...
Side 12
... standard . Once the Commission has initiated development of a standard ( the development period will normally be 150 days ) , it then has 210 days in which to publish a pro- posed standard or withdraw the notice . This period may be ...
... standard . Once the Commission has initiated development of a standard ( the development period will normally be 150 days ) , it then has 210 days in which to publish a pro- posed standard or withdraw the notice . This period may be ...
Side 13
... standard being considered must be taken into account . • The public is to be given full opportunity to play a major role in the development of standards . • All segments to be affected by a standard are to be represented in the process ...
... standard being considered must be taken into account . • The public is to be given full opportunity to play a major role in the development of standards . • All segments to be affected by a standard are to be represented in the process ...
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acupuncture Advertising and sale Animal Drug Application article's blood Bureau Calif Charged chemical Colo color Consent decree authorized consumer safety officer consumer specialists contents declaration contents statement Cosmetic Act court decree authorized release decree ordered destruction Default decree ordered diet dietary diethylstilbestrol display panel area Dist District Drug Application effective Fair Packaging false and misleading FDA CONSUMER FDA's Federal Federal Food food additive Food and Drug Government hazardous substances Health held for sale held under insanitary ingredients insanitary conditions inspection label lacked label statements Labeling Act Laboratories laser manufacturer medicines ment methadone misleading claims nolo contendere Notices of Judgment nutrients over-the-counter drugs P.O. Box pacemaker Packaging and Labeling packed percent pesticide poisonous prescription principal display panel protein quantity of contents regulations rodent safe sale by mail Salmonella shipped shipper sumer tablets tion type size less vaccine violation vitamin vitamin E
Populære avsnitt
Side 4 - ... if it consists in whole or in part of any filthy, putrid, or decomposed substance, or if it is otherwise unfit for food; or (4) if it has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health...
Side 36 - Institute, said that his resolution is a "factual nonemotional" approach. He based his figure on the 1968 dietary allowances of the Food and Nutrition Board of the National Academy of Sciences and the estimated city retail food prices of the Bureau of Labor Statistics.
Side 19733 - PUBLICITY SEC. 705. (a) The Secretary shall cause to be published from time to time reports summarizing all judgments, decrees, and court orders which have been rendered under this Act, including the nature of the charge and the disposition thereof.
Side 6 - The cases generally involve foods, drugs, devices, or cosmetics which were alleged to be adulterated or misbranded or otherwise violative of the law when introduced into and while in interstate commerce, or while held for sale after shipment in interstate commerce.
Side 5 - Act, including the nature of the charge and the disposition thereof. (b) The Secretary may also cause to be disseminated information regarding food, drugs, devices, or cosmetics in situations involving, in the opinion of the Secretary, imminent danger to health or gross deception of the consumer.
Side 35 - No claim may be made that a food is a significant source of a nutrient unless that nutrient is present in the food at a level equal to or in excess of 10 percent of the US RDA in a serving (portion).
Side 38 - substantial evidence" means evidence consisting of adequate and wellcontrolled investigations including clinical investigations by experts qualified by scientific training and experience to evaluate the effectiveness of the drug involved.
Side 17 - laser" stands for Light Amplification by Stimulated Emission of Radiation.
Side 30 - The law defines a cosmetic as misbranded: if its labeling is false or misleading in any particular; if it is in package form, unless it bears a label containing the name and place of business of the manufacturer, packer or distributor, and an accurate statement of the quantity of the contents in terms of weight, measure or numerical count...