ECU Libraries Catalog

Guidance for industry : clinical pharmacology section of labeling for human prescription drug and biological products : content and format.

Other author/creatorCenter for Drug Evaluation and Research (U.S.)
Other author/creatorCenter for Biologics Evaluation and Research (U.S.)
Format Electronic and Book
Publication InfoRockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER) : Center for Biologics Evaluation and Research (CBER), [2009]
Description11 pages : digital, PDF file.
Supplemental Content http://purl.access.gpo.gov/GPO/LPS110438
Subject(s)
Portion of title Clinical pharmacology section of labeling for human prescription drug and biological products
General noteTitle from title screen (viewed on Mar. 19, 2009).
General note"Draft guidance."
General note"February 2009."
Technical detailsMode of access: Internet at the FDA.Web site. Address as of 3/19/09: http://www.fda.gov/cder/guidance/1923dft.pdf ; current access is available via PURL.
GPO item number0499-T-02 (online)
Govt. docs number HE 20.4802:P 49

Available Items

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