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  1. 1
    Q4B evaluation and recommendation of pharmacopoeial texts for use in the ICH regions : annex 5, disintegration test general chapter.
    Published 2008
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    Government Document Conference Proceeding eBook
  2. 2
    E2f development safety update report.
    Published 2008
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    Government Document Conference Proceeding 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
    Guidance for industry : S1C(R2) dose selection for carcinogenicity studies.
    Published 2008
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    Government Document Conference Proceeding eBook
  5. 5
    Evaluation and recommendation of pharmacopoeial texts for use in the ICH regions on Uniformity of Dosage Units, General Chapter.
    Published 2008
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    Government Document Conference Proceeding eBook
  6. 6
    Evaluation and recommendation of pharmacopoeial texts for use in the ICH regions on Dissolution Test General Chapter.
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    Government Document Conference Proceeding eBook
  7. 7
    Evaluation and recommendation of pharmacopoeial texts for use in the ICH regions on Sterility Test General Chapter.
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    Government Document Conference Proceeding eBook
  8. 8
    S9 nonclinical evaluation for anticancer pharmaceuticals.
    Published 2009
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    Government Document Conference Proceeding eBook
  9. 9
    Guidance for industry : Q4B evaluation and recommendation of pharmacopoeial texts for use in the ICH regions : annex 2 test for extractable volume of parenteral preparations general chapter.
    Published 2009
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    Government Document Conference Proceeding eBook
  10. 10
    Guidance for industry : Q4B evaluation and recommendation of pharmocopoeial texts for use in the ICH regions : annex 3 test for particulate contamination, subdivisible particles general chapter.
    Published 2009
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    Government Document Conference Proceeding eBook
  11. 11
    Guidance for industry : M2 eCTD : electronic common technical document specification.
    Published 2003
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    Government Document Conference Proceeding eBook
  12. 12
    Guidance for industry M2 : eCTD specification : questions & answers and change requests.
    Published 2005
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    Government Document Conference Proceeding eBook
  13. 13
    Guidance for industry : M4, the CTD, efficacy questions and answers.
    Published 2004
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    Government Document Conference Proceeding eBook
  14. 14
    Guidance for industry : M4, the CTD, general questions and answers.
    Published 2004
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    Government Document Conference Proceeding eBook
  15. 15
    Guidance for industry : Q3A impurities in new drug substances.
    Published 2008
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    Government Document Conference Proceeding eBook
  16. 16
    Guidance for industry : Q3B(R2) impurities in new drug products.
    Published 2006
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    Government Document Conference Proceeding eBook
  17. 17
    Guidance for industry : Q2B validation of analytical procedures, methodology.
    Published 1996
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    Government Document Conference Proceeding eBook
  18. 18
    Guidance for industry : Q1E evaluation of stability data.
    Published 2004
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    Government Document Conference Proceeding eBook
  19. 19
    Guidance for industry : Q1A(R2) stability testing of new drug substances and products.
    Published 2003
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    Government Document Conference Proceeding eBook
  20. 20
    Guidance for industry : Q3C tables and list.
    Published 2003
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    Government Document Conference Proceeding eBook
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