Showing 1 - 18 results of 18 for search '"Therapeutics"', query time: 0.23s Refine Results
  1. 1
    Guidance for industry : available therapy.
    Published 2004
    Subjects: “...Therapeutics Government policy United States....”
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    Government Document eBook
  2. 2
    Guidance for industry : food-effect bioavailability and fed bioequivalence studies.
    Published 2002
    Subjects: “...Drugs Therapeutic equivalency....”
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    Government Document eBook
  3. 3
    Guidance for industry : statistical approaches to establishing bioequivalence.
    Published 2001
    Subjects: “...Drugs United States Therapeutic equivalency....”
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    Government Document eBook
  4. 4
    Guidance : topical dermatologic corticosteroids, in vivo bioequivalence.
    Published 1995
    Subjects: “...Drugs United States Therapeutic equivalency....”
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    Government Document eBook
  5. 5
    Guidance for industry : monoclonal antibodies used as reagents in drug manufacturing.
    Published 2001
    Subjects: “...Monoclonal antibodies Therapeutic use United States....”
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    Government Document eBook
  6. 6
    Guidance for industry : submission of summary bioequivalence data for ANDAs.
    Published 2009
    Subjects: “...Drugs United States Therapeutic equivalency....”
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    Government Document eBook
  7. 7
    Guidance for industry : assay development for immunogenicity testing of therapeutic proteins.
    Published 2009
    Subjects: “...Proteins Therapeutic use Testing....”
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    Government Document eBook
  8. 8
    Guidance for indusry : bioavailability and bioequivalence studies for nasal aerosols and nasal sprays for local action.
    Published 2003
    Subjects: “...Drugs United States Therapeutic equivalency....”
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    Government Document eBook
  9. 9
    Guidance for industry : SUPAC-MR : modified release solid oral dosage forms : scale-up and postapproval changes, chemistry, manufacturing and controls, in vitro dissolution testing and in vivo bioequivalence documentation.
    Published 1997
    Subjects: “...Drugs Therapeutic equivalency Documentation United States....”
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    Government Document eBook
  10. 10
    Guidance for industry : nonsterile semisolid dosage forms : scale-up and postapproval changes : chemistry, manufacturing, and controls : in vitro release testing and in vivo bioequivalence documentation.
    Published 1997
    Subjects: “...Drugs Therapeutic equivalency Documentation United States....”
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    Government Document eBook
  11. 11
    Guidance for industry : clozapine tables, in vivo bioequivalence and in vitro dissolution testing.
    Published 2005
    Subjects: “...Drugs United States Therapeutic equivalency....”
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    Government Document eBook
  12. 12
    Guidance for industry : waiver of in vivo bioavailability studies for immediate-release soild oral dosage forms based on a biopharmaceutics classification system.
    Published 2000
    Subjects: “...Drugs United States Therapeutic equivalency....”
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    Government Document eBook
  13. 13
    Guidance for industry : interpreting sameness of monoclonal antibody products under the orphan drug regulations.
    Published 1999
    Subjects: “...Monoclonal antibodies Therapeutic use Government policy United States....”
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    Government Document eBook
  14. 14
    Guidance for industry : immediate release solid oral dosage forms : scale-up and postapproval changes, chemistry, manufacturing and controls, in vitro dissolution testing, and in vivo bioequivalence documentation.
    Published 1995
    Subjects: “...Drugs Therapeutic equivalency Documentation United States....”
    Get full text
    Government Document eBook
  15. 15
    Guidance for industry : handling and retention of BA and BE testing samples.
    Published 2004
    Subjects: “...Drugs Therapeutic equivalency Testing Government policy United States....”
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    Government Document eBook
  16. 16
    Guidance for industry : comparability protocols, protein drug products and biological products; chemistry, manufacturing, and controls information.
    Published 2003
    Subjects: “...Biological products Therapeutic use United States....”
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    Government Document eBook
  17. 17
    Approved drug products with therapeutic equivalence evaluations.
    Published 1985
    Subjects: “...Drugs Therapeutic equivalency Periodicals....”
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    Government Document Microform Serial
  18. 18
    Approved drug products with therapeutic equivalence evaluations.
    Subjects: “...Drugs Therapeutic equivalency Periodicals....”
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    Government Document Serial
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