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ElectronicResource GovDoc

Title Draft guidance for HDE holders, institutional review boards (IRBs), clinical investigators, and FDA staff [electronic resource] : humanitarian device exemption regulation, questions and answers.

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

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4802:H 88    ---  Available
Description 20 p. : digital, PDF file
System Details Mode of access via the FDA CDER web site.
Note Title from PDF title page (viewed on Apr. 9, 2009).
"August 5, 2008."
Subject Medical instruments and apparatus.
Added Author Center for Devices and Radiological Health (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Added Title Humanitarian device exemption regulation, questions and answers
Gpo Item No. 0499-T-02 (online)
Sudoc No. HE 20.4802:H 88

 
    
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