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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

476 related items for PubMed ID: 10187558

  • 1. Investigational new drug applications; clinical holds--FDA. Direct final rule.
    Fed Regist; 1998 Dec 14; 63(239):68676-8. PubMed ID: 10187558
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  • 2. Investigational new drug applications; clinical holds; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Dec 14; 63(239):68710-2. PubMed ID: 10187560
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 6. 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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  • 8. 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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  • 10. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review--FDA. Direct final rule.
    Fed Regist; 1998 Apr 27; 63(80 Pt 1):20530-3. PubMed ID: 10179319
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  • 12. Skin protectant drug products for over-the-counter human use; astringent drug products; final monograph; direct final rule. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jun 13; 68(114):35290-3. PubMed ID: 12807133
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  • 15. Administrative practices and procedures; internal agency review of decisions; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Jun 16; 63(115):32772-4. PubMed ID: 10180279
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  • 17. Administrative practices and procedures; internal review of agency decisions---FDA. Direct final rule.
    Fed Regist; 1998 Jun 16; 63(115):32733-5. PubMed ID: 10180278
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  • 18. Medical devices; hearing aids; technical data amendments. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Jun 02; 73(106):31358-60. PubMed ID: 18677822
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  • 19. 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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