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  1. 1
    Guidance for industry : estimating the maximum safe starting dose in initial clinical trials for therapeutics in adult healthy volunteers.
    Published 2005
    Subjects: “...Drugs Dosage....”
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    Government Document eBook
  2. 2
    Drug bioequivalence : a report of the Office of Technology Assessment, Drug Bioequivalence Study Panel.
    Subjects: “...Drugs Bioavailability....”
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    Government Document eBook
  3. 3
    Papich handbook of veterinary drugs /
    by Papich, Mark G.
    Published 2021
    Subjects: “...Veterinary drugs....”
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    eBook
  4. 4
    Club drugs : a medical dictionary, bibliography and annotated research guide to Internet references /
    Published 2003
    Subjects: “...Designer drugs Computer network resources....”
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    eBook
  5. 5
    Guideline for industry : detection of toxicity to reproduction for medicinal products, addendum on toxicity to male fertility.
    Published 1996
    Subjects: “...Fertility Effect of drugs on....”
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    Government Document Conference Proceeding eBook
  6. 6
    Guidance for industry : food-effect bioavailability and fed bioequivalence studies.
    Published 2002
    Subjects: “...Drugs Bioavailability....”
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    Government Document eBook
  7. 7
    Detection of toxicity to reproduction for medicinal products.
    Published 1994
    Subjects: “...Fertility Effect of drugs on....”
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    Government Document Conference Proceeding eBook
  8. 8
    La respuesta del cerebro a los alucinógenos.
    Published 2006
    Subjects: “...Hallucinogenic drugs....”
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    Government Document eBook
  9. 9
    The depo-provera debate : hearings before the Select Committee on Population, U.S. House of Representatives, Ninety-fifth Congress, second session, August 8, 9, and 10, 1978.
    Published 1978
    Subjects: “...Contraceptive drugs....”
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    Government Document eBook
  10. 10
    Practical prescribing for medical students /
    Published 2014
    Subjects: “...Drugs Prescribing....”
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    eBook
  11. 11
    Guidance for industry : pharmacovigilance of veterinary medicinal products : management of periodical summary update reports (PSUs).
    Published 2001
    Subjects: “...Veterinary drugs....”
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    Government Document eBook
  12. 12
    Guidance for industry : dosage and administration section of labeling for human prescription drug and biological products, content and format.
    Published 2007
    Subjects: “...Drugs Labeling....”
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    Government Document eBook
  13. 13
    Guideline for the format and content of the nonclinical pharmacology/toxicology section of an application.
    Published 1987
    Subjects: “...Drugs United States Testing....”
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    Government Document eBook
  14. 14
    Special examiner of drugs, etc., Boston, Mass.
    Published 1884
    Subjects: “...Drugs....”
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    eBook
  15. 15
    Special examiner of drugs, at Philadelphia.
    Published 1902
    Subjects: “...Drugs....”
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    eBook
  16. 16
    Amending sections 303 (c) and 503 (b) of the Federal Food, Drug, and Cosmetic Act.
    Published 1951
    Subjects: “...Drugs....”
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    eBook
  17. 17
    Amending section 503 (b) of the Federal Food, Drug, and Cosmetic Act.
    Published 1951
    Subjects: “...Drugs....”
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    eBook
  18. 18
    Consideration of H.R. 3298.
    Published 1951
    Subjects: “...Drugs....”
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    eBook
  19. 19
    Extending certain narcotic drug provisions to Trust Territory of the Pacific Islands.
    Published 1953
    Subjects: “...Drugs....”
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  20. 20
    Extending certain narcotic drug provisions to Trust Territory of the Pacific Islands.
    Published 1953
    Subjects: “...Drugs....”
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    eBook
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