Food, Drug, Cosmetic Law Journal, Volume 31Commerce Clearing House, 1976 |
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Page 171
... authority to take action against adulterated cosmetics . The second point I would like to address is whether or not there is a demonstrated need for cosmetic GMPs , in light of current FDA authority and certain industry practices . All ...
... authority to take action against adulterated cosmetics . The second point I would like to address is whether or not there is a demonstrated need for cosmetic GMPs , in light of current FDA authority and certain industry practices . All ...
Page 396
... authority to promulgate regulations to further the general public health purposes of the Act.16 Thus , the FDA had come to assert a twofold claim of rule - mak- ing authority under Section 701 ( a ) : ( 1 ) the FDA cited Abbott for the ...
... authority to promulgate regulations to further the general public health purposes of the Act.16 Thus , the FDA had come to assert a twofold claim of rule - mak- ing authority under Section 701 ( a ) : ( 1 ) the FDA cited Abbott for the ...
Page 566
... authority . The Federal Authority would communicate the re - regis- tration of the foodstuff to each authority with jurisdiction over plants . or other establishments and thus the single re - registration would suffice.64 2.7.3 ...
... authority . The Federal Authority would communicate the re - regis- tration of the foodstuff to each authority with jurisdiction over plants . or other establishments and thus the single re - registration would suffice.64 2.7.3 ...
Contents
JOURNAL | 2 |
Current Topics in Canadian Drug Regulatory Affairs | 11 |
The Role of Microbiology in the Integrity of Foods | 17 |
Copyright | |
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94th Congress action adulterated advertising advisory Agency Agency's Amendments animal application authority bioavailability bioequivalence chemical Commissioner Committee compliance Congress consumer contains corporate Cosmetic Act cosmetic ingredient COSMETIC LAW JOURNAL Counsel Court criminal decision defendant dosage forms Drug Administration FDA Drug and Cosmetic drug application DRUG COSMETIC LAW Drug Law Institute drug products enforcement establish FDA's Federal Food food additives Food and Drug FOOD DRUG COSMETIC food law GMPs GRAS Health individual industry ingredient labeling investigations involved issue legislation manufacturer manufacturing practices medical device ment metic monograph nutrient nutritional Office package panel patient Pharmaceutical prescription drugs present problems procedure promulgated proposed prosecution recall recognized as safe regulations regulatory letter requirements responsibility result rule-making Schering-Plough Corporation scientific Section 305 hearing specific standards status statutory substances sumers tion tive United violation