Search Results - Center for Drug Evaluation and Research (U.S.)
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1
Manual del Centro para la Evaluacion e Investigacion de Farmacos
Published 2001“…Center for Drug Evaluation and Research (U.S.)…”
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Government Document Electronic eBook -
2
CDER ... report to the nation : improving public health through human drugs /
Published 1998“…Center for Drug Evaluation and Research (U.S.)…”
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Government Document Serial -
3
FDA Medical Library serials holdings list / by Bullock, Sylvia A.
Published 1995“…Center for Drug Evaluation and Research (U.S.)…”
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4
From test tube to patient improving health through human drugs /
Published 1999“…Center for Drug Evaluation and Research (U.S.)…”
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Government Document Electronic eBook -
5
Drugs@FDA
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Government Document Electronic eBook -
6
CDER ... report to the nation /
Published 1998“…Center for Drug Evaluation and Research (U.S.)…”
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7
Guideline on validation of the Limulus Amebocyte Lysate test as an end-product endotoxin test for human and animal parenteral drugs, biological products, and medical devices /
Published 1987“…Center for Drug Evaluation and Research (U.S.)…”
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8
Guideline for the study of drugs likely to be used in the elderly.
Published 1990“…Center for Drug Evaluation and Research (U.S.)…”
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9
FDA, Center for Drug Evaluation and Research : report to industry 1996.
Published 1997“…Center for Drug Evaluation and Research (U.S.)…”
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10
Report to industry.
Published 1997“…Center for Drug Evaluation and Research (U.S.)…”
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11
Drug safety newsletter.
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Government Document Journal -
12
From test tube to patient : protecting America's health through human drugs.
Published 2006“…Center for Drug Evaluation and Research (U.S.)…”
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Government Document eBook -
13
E 16 genomic biomarkers related to drug response context, structure, and format of qualification submissions.
Published 2009“…Center for Drug Evaluation and Research (U.S.)…”
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14
Guidance for industry bioavailability and bioequivalence studies for nasal aerosols and nasal sprays for local action.
Published 2003“…Center for Drug Evaluation and Research (U.S.)…”
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15
Guidance for industry submission of summary bioequivalence data for ANDAs.
Published 2009“…Center for Drug Evaluation and Research (U.S.)…”
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16
Guidance for industry nasal spray and inhalation solution, suspension, and spray drug products : chemistry, manufacturing, and controls documentation.
Published 2002“…Center for Drug Evaluation and Research (U.S.)…”
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17
Guidance for industry SUPAC-IR/MR : immediate release and modified release solid oral dosage forms : manufacturing equipment addendum.
Published 1999“…Center for Drug Evaluation and Research (U.S.)…”
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18
Guidance for industry handling and retention of BA and BE testing samples.
Published 2004“…Center for Drug Evaluation and Research (U.S.)…”
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19
Guidance for industry liposome drug products, chemistry, manufacturing, and controls; human pharmacokinetics and bioavailablity; and labeling documentation.
Published 2002“…Center for Drug Evaluation and Research (U.S.)…”
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20
Guidance for industry expiration dating and stability testing of solid oral dosage form drugs containing iron.
Published 1997“…Center for Drug Evaluation and Research (U.S.)…”
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Government Document Electronic eBook
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