Drug Safety, Parts 1-2U.S. Government Printing Office, 1964 |
From inside the book
Results 1-5 of 100
Page 6
... experience and the knowl- edge that our people have of where the trouble spots are apt to be results , hopefully , in our being able to choose our samples where they will do the most good . Mr. FOUNTAIN . After the subcommittee has had ...
... experience and the knowl- edge that our people have of where the trouble spots are apt to be results , hopefully , in our being able to choose our samples where they will do the most good . Mr. FOUNTAIN . After the subcommittee has had ...
Page 21
... experience OUTSIDE EXPERTS • Special problems Contributions by FDA and Government FDA OFFICE OF COMMISSIONER • Coordination and review • Issuance of regulations FDA SCIENTIFIC BUREAUS • Scientific evaluation ⚫Testing FDA BUREAU OF ...
... experience OUTSIDE EXPERTS • Special problems Contributions by FDA and Government FDA OFFICE OF COMMISSIONER • Coordination and review • Issuance of regulations FDA SCIENTIFIC BUREAUS • Scientific evaluation ⚫Testing FDA BUREAU OF ...
Page 25
... EXPERIENCED IN DESIGN AND INSTALLATION OF SCIENTIFIC DATA RETRIEVAL SYSTEMS • THE SYSTEM BEING DEVELOPED WILL INCLUDE ... experience in the design of informa- tion handling systems . The study is nearing completion . Realizing that any ...
... EXPERIENCED IN DESIGN AND INSTALLATION OF SCIENTIFIC DATA RETRIEVAL SYSTEMS • THE SYSTEM BEING DEVELOPED WILL INCLUDE ... experience in the design of informa- tion handling systems . The study is nearing completion . Realizing that any ...
Page 26
... Experience thus far , and the study by the Assistant Commissioner for Science Resources , have led FDA to adopt the ... experienced in advanced scientific information systems study FDA's overall scientific and medical com- munications ...
... Experience thus far , and the study by the Assistant Commissioner for Science Resources , have led FDA to adopt the ... experienced in advanced scientific information systems study FDA's overall scientific and medical com- munications ...
Page 32
... experience from 1938 to 1962 showed the 1938 law to be defective in several important respects : The producer of a new drug did not have to establish that his drug would be effective , as well as safe , for its intended uses . We were ...
... experience from 1938 to 1962 showed the 1938 law to be defective in several important respects : The producer of a new drug did not have to establish that his drug would be effective , as well as safe , for its intended uses . We were ...
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Common terms and phrases
activities additional adequate adverse drug reactions adverse reactions advertisement Advisory agency American Medical Association animals antibiotic approved basic batch Chairman chemical chloramphenicol clinical investigations Commissioner of Food committee concerning contraindications Cosmetic Act Department of Health Drug Administration Drug Amendments drug application drug safety Education established name evaluation exemption experience facilities FDA's Federal Food Federal Register Food and Drug FOUNTAIN GOLDBERG Government GRAY hearing examiner hospitals HUSSEY ingredient inspection investigational drug labeling laboratory LARRICK manufacturing practice medical officers ment new-drug application operations package Packaging and labeling patients pharmaceutical industry Pharmaceutical Manufacturers Association pharmacology Pharmacy physicians prescription drug problems procedures processing proprietary name Public Health question records reports responsible safe samples scientific scientists side effects SMITH specific sponsor staff Stat statement studies subcommittee submitted substance supplemental application therapeutic tion toxicity Welfare
Popular passages
Page 642 - ... 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 thereof.
Page 35 - ... 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 76 - 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 44 - States shall be exempt from the requirements of section 505 (a) of the Act if the following conditions are complied with: (1) The label of such drug bears the statement "CAUTION: NEW DRUG LIMITED BY FEDERAL (OR UNITED STATES) LAW TO INVESTIGATIONAL USE...
Page 301 - Section l(a) and is a necessary incentive to call forth private risk capital and expense to bring the invention to the point of practical application.
Page 470 - Chairman, shall leave title to such invention in the employee, subject, however, to the reservation to the Government of a nonexclusive, irrevocable, royalty-free license in the invention with power to grant licenses for all governmental purposes...
Page 578 - Secretary finds (1) that clinical or other experience, tests, or other scientific data show that such drug is unsafe for use under the conditions of use upon the basis of which the application was approved...
Page 119 - ... drug, based on a fair evaluation of all material facts, is false or misleading in any particular and...
Page 121 - ... when the agency for good cause finds (and incorporates the finding and a brief statement of reasons therefor in the rules issued) that notice and public procedure thereon are impracticable, unnecessary, or contrary to the public interest.
Page 320 - ... 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.