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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

542 related items for PubMed ID: 17674485

  • 1. Petition to request an exemption from 100 percent identity testing of dietary ingredients: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements. Interim final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Jun 25; 72(121):34959-69. PubMed ID: 17674485
    [Abstract] [Full Text] [Related]

  • 2. Current good manufacturing practice in manufacturing, packaging, labeling, or holding operations for dietary supplements. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Jun 25; 72(121):34751-958. PubMed ID: 17674484
    [Abstract] [Full Text] [Related]

  • 3. Proposed rule: current good manufacturing practice in manufacturing, packing, or holding dietary ingredients and dietary supplements.
    Melethil S.
    Life Sci; 2006 Mar 27; 78(18):2049-53. PubMed ID: 16516243
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  • 7. Current good manufacturing practice in manufacturing, processing, packing, or holding of drugs; revision of certain labeling controls--FDA. Final rule.
    Fed Regist; 1993 Aug 03; 58(147):41348-54. PubMed ID: 10127711
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  • 9. Prior notice of imported food under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Nov 07; 73(217):66293-410. PubMed ID: 19112701
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  • 11. Current good manufacturing practice regulation and investigational new drugs. Direct final rule.
    Food and Drug Administration. HHS.
    Fed Regist; 2006 Jan 17; 71(10):2458-62. PubMed ID: 16479693
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  • 12. Medical devices; current good manufacturing practice (CGMP) final fule; quality system regulation--FDA. Final rule.
    Fed Regist; 1996 Oct 07; 61(195):52602-62. PubMed ID: 10168287
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  • 14. Prevention of Salmonella enteritidis in shell eggs during production, storage, and transportation. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2009 Jul 09; 74(130):33029-101. PubMed ID: 19588581
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  • 16. Current good manufacturing practice for positron emission tomography drugs.
    Food and Drug Administration, HHS.
    Fed Regist; 2009 Dec 10; 74(236):65409-36. PubMed ID: 20169678
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  • 18. Establishment, maintenance, and availability of records: amendment to record availability requirements. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2014 Apr 04; 79(65):18799-802. PubMed ID: 24716304
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  • 19. Establishment and maintenance of records under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Dec 09; 69(236):71561-655. PubMed ID: 15586951
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