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Drug Industry Act of 1962 [electronic resource]: 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

United States. Congress. House. Committee on Interstate and Foreign Commerce
Format
Online; EBook; Government Document
Published
Washington : U.S. G.P.O., 1962.
Language
English
Series
ProQuest U.S. Congressional Hearings Digital Collection
SuDoc Number
Y 4.In 8/4:D 84
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.
Description
viii, 709 p. ; cm.
System requirements: PDF reader software.
Notes
  • Record is based on bibliographic data in ProQuest Congressional Hearings Digital Collection (last viewed Nov. 2009) Reuse except for individual research requires license from ProQuest, LLC.
  • Access to the Congressional Hearings Digital Collection is restricted by license to users on UVA's network. This document may also be available in print or microform at either UVa's Alderman or Law Libraries.
  • CIS No. HRG-1962-FCH-0019
  • Record is based on bibliographic data in ProQuest Congressional Hearings Digital Collection. Reuse except for individual research requires license from ProQuest, LLC.
Reproduction Notes
Electronic reproduction. [Bethesda, Md.] : ProQuest, 2004. digital, PDF file. ProQuest U.S. Congressional Hearings Digital Collection. Mode of access: World Wide Web via ProQuest website.
Copyright Not EvaluatedCopyright Not Evaluated
Technical Details
  • Staff View

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    a| Y 4.In 8/4:D 84
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    a| United States. b| Congress. b| House. b| Committee on Interstate and Foreign Commerce.
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    a| Drug Industry Act of 1962 h| [electronic resource] : b| 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.
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    a| Washington : b| U.S. G.P.O., c| 1962.
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    a| viii, 709 p. ; c| cm.
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    a| Record is based on bibliographic data in ProQuest Congressional Hearings Digital Collection (last viewed Nov. 2009) Reuse except for individual research requires license from ProQuest, LLC.
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    a| Access to the Congressional Hearings Digital Collection is restricted by license to users on UVA's network. This document may also be available in print or microform at either UVa's Alderman or Law Libraries.
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    a| CIS No. HRG-1962-FCH-0019
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    a| Record is based on bibliographic data in ProQuest Congressional Hearings Digital Collection. Reuse except for individual research requires license from ProQuest, LLC.
    520
      
      
    a| 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.
    520
      
      
    a| Considers (87) H.R. 11581, (87) H.R. 11582.
    533
      
      
    a| Electronic reproduction. b| [Bethesda, Md.] : c| ProQuest, d| 2004. e| digital, PDF file. n| ProQuest U.S. Congressional Hearings Digital Collection. n| Mode of access: World Wide Web via ProQuest website.
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    a| System requirements: PDF reader software.
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    a| Cosmetics x| Law and legislation z| United States.
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    a| Drugs x| Law and legislation z| United States.
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    a| Food law and legislation z| United States.
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    a| Medical instruments and apparatus x| Safety regulations z| United States.
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    i| Print version: a| United States. Congress. House. Committee on Interstate and Foreign Commerce. t| Drug Industry Act of 1962
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    i| Microfiche version: a| United States. Congress. House. Committee on Interstate and Foreign Commerce. t| Drug Industry Act of 1962. d| [Bethesda, Md.] : ProQuest,[2004] o| CIS Hrgs MF Gp 3--(87) H1931-6 w| (ProQuest)cis10701322
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    a| ProQuest U.S. Congressional Hearings Digital Collection.
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    u| http://proxy.its.virginia.edu/login?url=http://congressional.proquest.com/congcomp/getdoc?HEARING-ID=HRG-1962-FCH-0019 y| Electronic resource (PDF)
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    a| cis10701322
    040
      
      
    a| UMI c| UMI
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