Source:http://linkedlifedata.com/resource/pubmed/id/16794639
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2006-6-23
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pubmed:abstractText |
Despite the intense interest in biomarker development for cancer management, few biomarker assays for diagnostic uses have been submitted to the US Food and Drug Administration (FDA). What challenges must researchers overcome to bring cancer-detection technologies to the market and, therefore, into clinical use?
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1474-175X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
565-71
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pubmed:meshHeading |
pubmed-meshheading:16794639-Biological Assay,
pubmed-meshheading:16794639-Humans,
pubmed-meshheading:16794639-Marketing,
pubmed-meshheading:16794639-Neoplasms,
pubmed-meshheading:16794639-Reagent Kits, Diagnostic,
pubmed-meshheading:16794639-Tumor Markers, Biological,
pubmed-meshheading:16794639-United States,
pubmed-meshheading:16794639-United States Food and Drug Administration
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pubmed:year |
2006
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pubmed:articleTitle |
The US Food and Drug Administration perspective on cancer biomarker development.
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pubmed:affiliation |
Office of in vitro Diagnostic Devices, Center for Devices and Radiological Health, Food and Drug Administration, NFZ-440, 2098 Gaither Road, Rockville, Maryland 20857, USA. steve.gutman@fda.hhs.gov
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pubmed:publicationType |
Journal Article,
Review
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