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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

505 related items for PubMed ID: 11010654

  • 1. Amendment of various device regulations to reflect current American Society for Testing and Material citations. Food and Drug Administration, HHS. Direct final rule.
    Fed Regist; 2000 Jan 24; 65(15):3584-5. PubMed ID: 11010654
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  • 2. Medical devices; establishment registration and device listing for manufacturers and distributors of devices--FDA. Direct final rule.
    Fed Regist; 1998 Sep 29; 63(188):51825-7. PubMed ID: 10185812
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  • 3. Quality mammography standards. Department of Health and Human Services (HHS), Public Health Service (PHS), Food and Drug Administration (FDA). Direct final rule.
    Fed Regist; 1999 Jun 17; 64(116):32404-7. PubMed ID: 10558582
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  • 6. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule.
    Fed Regist; 1998 May 12; 63(91):26069-77. PubMed ID: 10179334
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  • 10. Amendment to examination and investigation sample requirements--FDA. Direct final rule.
    Fed Regist; 1998 Sep 25; 63(186):51297-9. PubMed ID: 10185810
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  • 11. Amendment to the current good manufacturing practice regulations for finished pharmaceuticals. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Dec 04; 72(232):68064-70. PubMed ID: 18064770
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  • 14. Medical devices; reprocessed single-use devices; requirement for submission of validation data. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Sep 25; 71(185):55729-37. PubMed ID: 17017469
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  • 15. Amendments to general regulations of the Food and Drug Administration. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2010 Nov 30; 75(229):73951-5. PubMed ID: 21121182
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  • 16. Revisions to the general safety requirements for biological products--FD. Direct final rule.
    Fed Regist; 1998 Apr 20; 63(75):19399-403. PubMed ID: 10178869
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  • 17. Revision of requirements applicable to albumin (human), plasma protein fraction (human), and immune globulin (human). Food and Drug Administration, HHS. Direct final rule.
    Fed Regist; 1999 May 14; 64(93):26282-7. PubMed ID: 10558530
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  • 19. 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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  • 20. Revision to requirements for licensed Anti-Human Globulin and Blood Grouping Reagents. Food and Drug Administration, HHS. Direct final rule.
    Fed Regist; 2000 Dec 12; 65(239):77497-9. PubMed ID: 11503726
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