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Title Guidance for industry [electronic resource] : providing regulatory submissions in electronic format : human pharmaceutical product applications and related submissions using the eCTD specifications.

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

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4802:R 26/3    ---  Available
Description ii, 16 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).
"June 2008."
"Revision 2."
Subject Drug approval -- United States.
Electronic filing systems -- United States.
Center for Drug Evaluation and Research (U.S.)
Added Author Center for Biologics Evaluation and Research (U.S.)
Added Title Providing regulatory submissions in electronic format
Human pharmaceutical product applications and related submissions using the eCTD specifications
Gpo Item No. 0499-T-02 (online)
Sudoc No. HE 20.4802:R 26/3

 
    
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