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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

1315 related items for PubMed ID: 19112701

  • 1. 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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  • 2. Registration of food facilities under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2005 Oct 03; 70(190):57505-9. PubMed ID: 16200686
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  • 3. 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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  • 8. 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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  • 9. Medical devices; reports of corrections and removals--FDA. Direct final rule.
    Fed Regist; 1998 Aug 07; 63(152):42229-33. PubMed ID: 10181725
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  • 11. Year 2000 (Y2K) computer compliance guide; guidance for FDA personnel. Food and Drug Administration. Notice.
    Fed Regist; 1999 May 14; 64(93):26424-6. PubMed ID: 10558534
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  • 14. 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
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  • 15. 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
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  • 16. Foreign establishment registration and listing. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 Nov 27; 66(228):59138-61. PubMed ID: 11776289
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  • 20. Medical devices; implementation of third party review under the Food and Drug Administration Modernization Act of 1997; emergency processing request under OMB review--FDA. Notice.
    Fed Regist; 1998 May 22; 63(99):28388-91. PubMed ID: 10179874
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