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Journal Abstract Search

140 related items for PubMed ID: 11661757

  • 1. Changing federal regulation of IRB's, part II: DHEW's and FDA's proposed regulations.
    Levine RJ.
    IRB; 1979 Nov; 1(7):1-5+. PubMed ID: 11661757
    [No Abstract] [Full Text] [Related]

  • 2. Changing federal regulation of IRB's: the Commission's recommendations and the FDA's proposals.
    Levine RJ.
    IRB; 1979 Mar; 1(1):1-3+. PubMed ID: 11662736
    [No Abstract] [Full Text] [Related]

  • 3. Advice on compensation: one IRB's response to DHEW's 'interim final regulation'.
    Levine RJ.
    IRB; 1979 Mar; 1(1):5. PubMed ID: 11662737
    [No Abstract] [Full Text] [Related]

  • 4. Reflections on the FDA's intraocular lens regulations.
    Worthen DM.
    IRB; 1980 Apr; 2(4):1-3. PubMed ID: 11661783
    [No Abstract] [Full Text] [Related]

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  • 6. The FDA's final regulations: IRBs and medical devices.
    Holder AR.
    IRB; 1980 Apr; 2(6):1-4. PubMed ID: 11661803
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  • 11. The FDA's response to AIDS: paradigm shift in new drug policy?
    Podraza R.
    Food Drug Law J; 1993 Apr; 48(3):351-75. PubMed ID: 11653267
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  • 12. Advice on compensation: more responses to DHEW's 'interim final regulation'.
    Levine RJ.
    IRB; 1979 Apr; 1(2):5-7. PubMed ID: 11661642
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  • 14. IRB workloads and misleading statistics.
    Maloney DM.
    Hum Res Rep; 1998 Oct; 13(10):3. PubMed ID: 11657740
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  • 16. Task force finalizes genetic testing recommendations.
    Nat Biotechnol; 1997 Apr; 15(4):300. PubMed ID: 11644941
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  • 20. The regulation of clinical investigators.
    Endries RN.
    Food Drug Cosmet Law J; 1980 Jul; 35(7):415-23. PubMed ID: 11661860
    [No Abstract] [Full Text] [Related]

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