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Title Guidance for industry [electronic resource] : pharmacogenomic data submissions, companion evidence.

Imprint Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : National Center for Toxicological Research : Center for Biologics Evaluation and Research : Center for Devices and Radiological Research, [2007]

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4702:P 49/10    ---  Available
Description 25 p. : digital, PDF file
System Details Mode of access via the FDA web site.
Note Title from PDF title page (viewed on June 2, 2009).
"Draft guidance."
"Procedural."
"August 2007."
Subject Pharmacogenomics -- Government policy -- United States.
Added Author Center for Drug Evaluation and Research (U.S.)
National Center for Toxicological Research.
Center for Biologics Evaluation and Research (U.S.)
Center for Devices and Radiological Health (U.S.)
Added Title Pharmacogenomic data submissions, companion evidence
Gpo Item No. 0499-T (online)
Sudoc No. HE 20.4702:P 49/10

 
    
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