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PUBMED FOR HANDHELDS

Journal Abstract Search


304 related items for PubMed ID: 10558407

  • 21. 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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  • 24. International Conference on Harmonisation; guidance on quality of biotechnological/biological products: derivation and characterization of cell substrates used for production of biotechnological/biological products; availability. Notice. Food and Drug Administration, HHS.
    Fed Regist; 1998 Sep 21; 63(182):50244-9. PubMed ID: 12269373
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  • 26. Medical physicists role under MQSA (Mammography Quality Standards Act).
    Haus AG.
    Adm Radiol; 1994 Nov 21; 13(11):35-8. PubMed ID: 10139208
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  • 28. Quality mammography standards; correction--FDA. Final rule; correction.
    Fed Regist; 1997 Nov 10; 62(217):60614-32. PubMed ID: 10177320
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  • 30. Immunotoxicity testing guidance; availability. Food and Drug Administration, HHS. Notice.
    Fed Regist; 1999 May 06; 64(87):24408-9. PubMed ID: 10558489
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  • 32. Breast imaging: why MQSA (Mammography Quality Standards Act).
    Kneece J.
    Adm Radiol; 1994 Nov 06; 13(11):33-4. PubMed ID: 10139207
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  • 33. Quality assurance in nuclear medicine facilities; availability of final recommendations--FDA. Notice.
    Fed Regist; 1985 May 13; 50(92):20011-2. PubMed ID: 10271280
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  • 34. International Conference on Harmonisation; guidance on Q8(R1) Pharmaceutical Development; addition of annex; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2009 Jun 09; 74(109):27325-6. PubMed ID: 19588572
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  • 35. "Guidance for Industry: On the Content and Format of Chemistry, Manufacturing and Controls Information and Establishment Description Information for an Allergenic Extract or Allergen Patch Test"; availability. Food and Drug Administration, HHS. Notice.
    Fed Regist; 1999 Apr 23; 64(78):20006-7. PubMed ID: 10558479
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  • 36. International Conference on Harmonisation; guidance on good manufacturing practice for active pharmaceutical ingredients; availability. Notice.
    Food and Drug Administration, HHS.
    Fed Regist; 2001 Sep 25; 66(186):49028-9. PubMed ID: 12358036
    [Abstract] [Full Text] [Related]

  • 37. Regulations for in vivo radiopharmaceuticals used for diagnosis and monitoring. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 May 17; 64(94):26657-70. PubMed ID: 10558516
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  • 39. Medical devices; performance standard for diagnostic x-ray systems; amendment. Department of Health and Human Services (HHS), Public Health Service (PHS), Food and Drug Administration (FDA). Final rule.
    Fed Regist; 1999 Jul 02; 64(127):35924-8. PubMed ID: 10558580
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  • 40. The Mammography Quality Standards Act of 1992. History and philosophy.
    Houn F, Elliott ML, McCrohan JL.
    Radiol Clin North Am; 1995 Nov 02; 33(6):1059-65. PubMed ID: 7480655
    [Abstract] [Full Text] [Related]


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