In vitro diagnostic (IVD) device studies, frequently asked questions.

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Bibliographic Details
Imprint:	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health : Center for Biologics Evaluation and Research, [2007]
Description:	1 online resource (ii, 46 pages) : digital, PDF file
Language:	English
Subject:	Toxicity testing -- In vitro -- United States. Medical instruments and apparatus -- United States -- Testing.
Format:	E-Resource U.S. Federal Government Document Book
URL for this record:	http://pi.lib.uchicago.edu/1001/cat/bib/7730967

Hidden Bibliographic Details
Varying Form of Title:	At head of title: Draft guidance for industry and FDA staff
Other authors / contributors:	Center for Devices and Radiological Health (U.S.) Center for Biologics Evaluation and Research (U.S.)
Notes:	Title from PDF title page (viewed on May 4, 2009). "Document issued on: October 25, 2007". Includes bibliographical references: (pages 30-32).
GPO item no.:	0499-T-02 (online)
Govt.docs classification:	HE 20.4802:V 83/2/DRAFT

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