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  1. 1
    Guidance for industry : indexing structured product labeling.
    Published 2008
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    Government Document eBook
  2. 2
    Guidance for industry : clinical pharmacology section of labeling for human prescription drug and biological products : content and format.
    Published 2009
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    Government Document eBook
  3. 3
    Guidance for industry : contents of a complete submission for the evaluation of proprietary names.
    Published 2008
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    Government Document eBook
  4. 4
    Guidance for industry : patient-reported outcome measures, use in medical product development to support labeling claims.
    Published 2006
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    Government Document eBook
  5. 5
    Guidance for industry : label comprehension studies for nonprescription drug products : draft guidance.
    Published 2009
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    Government Document eBook
  6. 6
    Guidance for industry : clinical lactation studies; study design, data analysis, and recommendations for labeling.
    Published 2005
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    Government Document eBook
  7. 7
    Guidance for industry : clinical studies section of labeling for human prescription drug and biological products, content and format.
    Published 2006
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    Government Document eBook
  8. 8
    Guidance for industry : providing regulatory submissions in electronic format, content of labeling.
    Published 2005
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    Government Document eBook
  9. 9
    Guidance for industry : SPL standard for content of labeling technical Qs & As.
    Published 2009
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    Government Document eBook
  10. 10
    Guidance for industry : providing regulatory submissions in electronic format, prescription drug advertising and promotional labeling.
    Published 2001
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    Government Document eBook
  11. 11
    Guidance for industry : noncontraceptive estrogen drug products for the treatment of vasomotor symptoms and vulvar and vaginal atrophy symptoms : recommended prescribing information for health care providers and patient labeling.
    Published 2005
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    Government Document eBook
  12. 12
    Guidance for industry : public availability of labeling changes in "changes being effected" supplements.
    Published 2006
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    Government Document eBook
  13. 13
    Guidance for industry : referencing discontinued labeling for listed drugs in abbreviated new drug applications.
    Published 2000
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    Government Document eBook
  14. 14
    Guidance for industry : warnings and precautions, contraindications, and boxed warning sections of labeling for human prescription drug and biological products, content and format.
    Published 2006
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    Government Document eBook
  15. 15
    Guidance for industry : implementation of Section 126 of the Food and Drug Administration Modernization Act of 1997, elimination of certain labeling requirements.
    Published 1998
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    Government Document eBook
  16. 16
    Guidance for industry : national uniformity for nonprescription drugs : ingredient listing for OTC drugs.
    Published 1998
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    Government Document eBook
  17. 17
    Guidance for industry : adverse reactions section of labeling for human prescription drug and biological products, content and format.
    Published 2006
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    Government Document eBook
  18. 18
    Guidance for industry : content and format for geriatric labeling.
    Published 2001
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    Government Document eBook
  19. 19
    Guidance for industry : dosage and administration section of labeling for human prescription drug and biological products, content and format.
    Published 2007
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    Government Document eBook
  20. 20
    Guidance for industry : hypertension indication, drug labeling for cardiovascular outcome claims.
    Published 2008
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    Government Document eBook
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