Drug Industry Act of 1962 : hearings before the United States House Committee on Interstate and Foreign Commerce, Eighty-Seventh Congress, second session, on June 19-22, Aug. 20-23, 1962.

Considers the following bills to amend the Federal Food, Drug, and Cosmetic Act. H.R. 11581, the Drug and Factory Inspection Amendments of 1962, to require manufacturers to follow certain research, production and marketing safety procedures. H.R. 11582, the Cosmetics and Therapeutic Devices Amendmen...

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Bibliographic Details
Corporate Authors:	United States. Congress. House. Committee on Interstate and Foreign Commerce, ProQuest (Firm)
Format:	Government Document eBook
Language:	English
Published:	Washington : U.S. G.P.O., 1962.
Series:	U.S. Congressional Hearings.
Subjects:	Cosmetics > Law and legislation > United States. Drugs > Law and legislation > United States. Food law and legislation > United States. Medical instruments and apparatus > Safety regulations > United States. Electronic books.
Online Access:	Connect to the full text of this electronic book

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Summary:	Considers the following bills to amend the Federal Food, Drug, and Cosmetic Act. H.R. 11581, the Drug and Factory Inspection Amendments of 1962, to require manufacturers to follow certain research, production and marketing safety procedures. H.R. 11582, the Cosmetics and Therapeutic Devices Amendments of 1962, to require safety certification for cosmetics and medical devices; to require labeling on containers containing hazardous substances; and to strengthen controls on food and animal feed additives. Considers (87) H.R. 11581, (87) H.R. 11582.
Item Description:	Record is based on bibliographic data in ProQuest Congressional Hearings Digital Collection. Reuse except for individual research requires license from ProQuest, LLC. Electronic resource.
Physical Description:	1 online resource.
Format:	System requirements: PDF reader software.