16900132

Source:http://linkedlifedata.com/resource/pubmed/id/16900132

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220905, umls-concept:C0687640
pubmed:issue	8
pubmed:dateCreated	2006-8-10
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9604648
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1087-0156
pubmed:author	pubmed-author:GottliebScottS, pubmed-author:WoodcockJanetJ
pubmed:issnType	Print
pubmed:volume	24
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	927-9
pubmed:meshHeading	pubmed-meshheading:16900132-Device Approval, pubmed-meshheading:16900132-Diagnostic Techniques and Procedures, pubmed-meshheading:16900132-Drug Approval, pubmed-meshheading:16900132-Government Regulation, pubmed-meshheading:16900132-United States, pubmed-meshheading:16900132-United States Food and Drug Administration
pubmed:year	2006
pubmed:articleTitle	A regulatory perspective on in vitro diagnostics.
pubmed:affiliation	U.S. Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, USA.
pubmed:publicationType	Journal Article