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 26
... procedures , such as the processing of petitions , review of plans for clinical testing of new drugs , the approval of new drugs , the establishment of tolerances , the issuance of regula- tions , and the conduct of hearings ; second ...
... procedures , such as the processing of petitions , review of plans for clinical testing of new drugs , the approval of new drugs , the establishment of tolerances , the issuance of regula- tions , and the conduct of hearings ; second ...
Page 27
... procedures used by the manufacturer and the evidence of safety and effectiveness of the product for its intended use but also the truthfulness of the proposed labeling . In addition to the work the Bureau of Medicine does with respect ...
... procedures used by the manufacturer and the evidence of safety and effectiveness of the product for its intended use but also the truthfulness of the proposed labeling . In addition to the work the Bureau of Medicine does with respect ...
Page 33
... procedures in this vital area of scientific information exchange , FDA has studied systems employed by drug firms and by organizations involved in abstracting scientific journals , it has studied systems employed by the National Library ...
... procedures in this vital area of scientific information exchange , FDA has studied systems employed by drug firms and by organizations involved in abstracting scientific journals , it has studied systems employed by the National Library ...
Page 54
... procedures . The revised regulations make clear that the planning of the first two phases may be considerably less detailed than that of phase 3 and that the investigator in the early phases may pursue promising leads that may emerge ...
... procedures . The revised regulations make clear that the planning of the first two phases may be considerably less detailed than that of phase 3 and that the investigator in the early phases may pursue promising leads that may emerge ...
Page 61
... procedures outlined in § 130.3 of this chapter are complied with . For the purposes of this section , the references in § 130.3 of this chapter to " new drug " and " approved new - drug application " shall be deemed to read " antibiotic ...
... procedures outlined in § 130.3 of this chapter are complied with . For the purposes of this section , the references in § 130.3 of this chapter to " new drug " and " approved new - drug application " shall be deemed to read " antibiotic ...
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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.