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  1. 1
    E2f development safety update report.
    Published 2008
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    Government Document Conference Proceeding eBook
  2. 2
    Guidance for industry : fast track drug development programs, designation, development and application review.
    Published 2006
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    Government Document eBook
  3. 3
    Guidance for industry : Q3A impurities in new drug substances.
    Published 2008
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    Government Document Conference Proceeding eBook
  4. 4
    Q8(R1) pharmaceutical development revision 1.
    Published 2008
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    Government Document eBook
  5. 5
    Guidance for industry : Q3B(R2) impurities in new drug products.
    Published 2006
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    Government Document Conference Proceeding eBook
  6. 6
    Guidance for industry : S7A safety pharmacology studies for human pharmaceuticals.
    Published 2001
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    Government Document Conference Proceeding eBook
  7. 7
    Guidance for industry : E2E pharmacovigilance planning.
    Published 2005
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    Government Document Conference Proceeding eBook
  8. 8
    Guidance for industry : premarketing risk assessment.
    Published 2005
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    Government Document eBook
  9. 9
    Guidance for industry : manufacturing, processing, or holding active pharmaceutical ingredients.
    Published 1998
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    Government Document eBook
  10. 10
    Guidance for industry : quality systems approach to pharmaceutical CGMP regulations.
    Published 2006
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    Government Document eBook
  11. 11
    Guidance for industry : population pharmacokinetics.
    Published 1999
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    Government Document eBook
  12. 12
    Guidance for industry : Q8(R2) pharmaceutical development.
    Published 2009
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    Government Document Conference Proceeding eBook
  13. 13
    Guidance for industry : fast track drug development programs, designation, development and application review.
    Published 2004
    Get full text
    Government Document eBook
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