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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

270 related items for PubMed ID: 22479732

  • 1. Current good manufacturing practice in manufacturing, processing, packing, or holding of drugs; revision of certain labeling controls. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2012 Mar 20; 77(54):16158-63. PubMed ID: 22479732
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  • 3. Toll-free number for reporting adverse events on labeling for human drug products. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Oct 28; 73(209):63886-97. PubMed ID: 19112682
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  • 5. 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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  • 6. Toll-free number for reporting adverse events on labeling for human drug products. Interim final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Jan 03; 73(2):402-4. PubMed ID: 18389912
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  • 8. Requirements on content and format of labeling for human prescription drug and biological products. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Jan 24; 71(15):3921-97. PubMed ID: 16479698
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  • 13. Delegations of authority and organization; issuance of written notices--FDA. Final rule.
    Fed Regist; 1992 May 01; 57(85):18823-4. PubMed ID: 10118461
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  • 14. 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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  • 15. Biological products: reporting of biological product deviations in manufacturing. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Nov 07; 65(216):66621-35. PubMed ID: 11503696
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