A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its AmendmentsU.S. Department of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, 1979 |
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Page 8
... issuance of three reports . based upon surveys made by the subcommittee . In the first of these reports , issued as House Report No. 1241 in September 1961 , we developed a comprehensive inventory of all con- sumer protection activities ...
... issuance of three reports . based upon surveys made by the subcommittee . In the first of these reports , issued as House Report No. 1241 in September 1961 , we developed a comprehensive inventory of all con- sumer protection activities ...
Page 26
... issuance of regula- tions , and the conduct of hearings ; second , because the nature of FDA's work demands high knowledge of and dependence upon scientific technology , medicine , law , and other complex disciplines . In addition , FDA ...
... issuance of regula- tions , and the conduct of hearings ; second , because the nature of FDA's work demands high knowledge of and dependence upon scientific technology , medicine , law , and other complex disciplines . In addition , FDA ...
Page 27
... Issuance of regulations FDA SCIENTIFIC BUREAUS Scientific evaluation • Testing FDA BUREAU OF MEDICINE Medical evaluations Monitoring of MDA's FDA DISTRICT OFFICE LABORATORIES Checks industry data Checks industry facilities and controls ...
... Issuance of regulations FDA SCIENTIFIC BUREAUS Scientific evaluation • Testing FDA BUREAU OF MEDICINE Medical evaluations Monitoring of MDA's FDA DISTRICT OFFICE LABORATORIES Checks industry data Checks industry facilities and controls ...
Page 31
... issued on June 10 , 1963 , and a final contract was signed on September 9 , 1963 , with Arthur D. Little , Inc. , of Cambridge , Mass . , an organization with experience in the design of informa- tion handling systems . The study is ...
... issued on June 10 , 1963 , and a final contract was signed on September 9 , 1963 , with Arthur D. Little , Inc. , of Cambridge , Mass . , an organization with experience in the design of informa- tion handling systems . The study is ...
Page 32
... issuance of regula- tions requiring sponsors of investigational drugs to report significant informa- tion to the Food and Drug Administration demonstrated clearly the need for a better way of handling the very basic and vital medical ...
... issuance of regula- tions requiring sponsors of investigational drugs to report significant informa- tion to the Food and Drug Administration demonstrated clearly the need for a better way of handling the very basic and vital medical ...
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Common terms and phrases
52 Stat additional adequate adverse drug reactions adverse reactions agency animal tests animals antibiotic approved Association batch Chairman changes chart chemical claimed investigational exemption clinical investigations clinical trials Commissioner of Food committee contained contraindications Cosmetic Act Department of Health distribution dosage form Drug Administration Drug Amendments drug application drug establishments DRUG SAFETY drugs for investigational Education established name evaluation experience facilities FDA's Federal Food Federal Register Food and Drug FOUNTAIN GOLDBERG Government GRAY hearing examiner industry ingredient inspection investigational drug June 20 labeling laboratory LARRICK manufacturing manufacturing practice ment methods new-drug application notified operations package Packaging and labeling paragraph patients pharmaceutical physicians prescription drug procedures processing proposed regulations proprietary name Public Health records registration reports request samples scientific scientists side effects specific sponsor statement studies subcommittee submitted supplemental application tion Welfare
Popular passages
Page 120 - ... substantial evidence" means evidence consisting of adequate and well-controlled investigations, including clinical investigations, by experts qualified by scientific training and experience to evaluate the effectiveness of the drug involved, on the basis of which it could fairly and responsibly be concluded by such experts that the drug will have the effect it purports or is represented to have under the conditions of use prescribed, recommended, or suggested in the labeling or proposed labeling...
Page 72 - State, unless the manufacturer, packer, or distributor thereof includes in all advertisements and other descriptive printed matter issued or caused to be issued by the manufacturer, packer, or distributor...
Page 489 - Comp., p. 456), provides in part: (a) The Government shall obtain the entire right, title and interest in and to all inventions made by any Government employee (1) during working hours, or (2) with a contribution by the Government of facilities, equipment, materials, funds, or information, or of time or services of other Government employees on official duty, or (3) which bear a direct relation to or are made in consequence of the official duties of the inventor.
Page 43 - ... a full list of the articles used as components of such drug; (3) a full statement of the composition of such drug; (4) a full description of the methods used in, and the facilities and controls used for, the manufacture, processing, and packing of such drug...
Page 120 - Secretary pursuant to subsection (b), do not include adequate tests by all methods reasonably applicable to show whether or not such drug is safe for use under the conditions prescribed, recommended, or suggested in the proposed labeling...
Page 329 - ... he should retain the principal or exclusive rights for a further period of time, the government shall have the right to require the granting of a license to an applicant on a non-exclusive royalty free basis.
Page 44 - Labeling on or within the package from which the drug is to be dispensed bears adequate information for its use, including indications, effects, dosages, routes, methods, and frequency and duration of administration, and any relevant hazards, contraindications, side effects, and precautions under which practitioners licensed by law to administer the drug can use the drug safely and for the purposes for which it is intended, including all purposes for which it is advertised or represented...
Page 131 - ... products conform to appropriate standards of identity, strength, quality, and purity. Laboratory controls shall include...
Page 99 - Part 132, that engage in the manufacture, preparation, propagation, compounding, or processing of a drug or drugs...
Page 114 - ... in sufficient detail to permit evaluation of the adequacy of the described methods of manufacture, processing, and packing and the described facilities and controls to determine and preserve the identity, strength, quality, and purity of the drug: a.