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Title Guidance for industry [electronic resource] : providing regulatory submissions in electronic format, postmarketing individual case safety reports.

Imprint Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2008]

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4802:R 26/2    ---  Available
Description 8 p. : digital, PDF file
System Details Mode of access via the FDA CBER web site.
Note Title from PDF title page (viewed on Apr. 23, 2009).
"Draft guidance".
"June 2008."
Subject Drug testing -- United States -- Case studies.
Electronic filing systems -- United States.
Added Author Center for Drug Evaluation and Research (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Added Title Providing regulatory submissions in electronic format, postmarketing individual case safety reports
Gpo Item No. 0499-T-02 (online)
Sudoc No. HE 20.4802:R 26/2

 
    
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