18027212

Source:http://linkedlifedata.com/resource/pubmed/id/18027212

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030351, umls-concept:C0043157, umls-concept:C0220938, umls-concept:C0557061, umls-concept:C1707689, umls-concept:C1883562, umls-concept:C2584313
pubmed:issue	6
pubmed:dateCreated	2007-11-20
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/18027212-18027208
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9200436
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	1054-3406
pubmed:author	pubmed-author:WangSue-JaneSJ
pubmed:issnType	Print
pubmed:volume	17
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1015-20; discussion 1029-32
pubmed:meshHeading	pubmed-meshheading:18027212-Bias (Epidemiology), pubmed-meshheading:18027212-Clinical Trials as Topic, pubmed-meshheading:18027212-Dose-Response Relationship, Drug, pubmed-meshheading:18027212-Drug Industry, pubmed-meshheading:18027212-Humans, pubmed-meshheading:18027212-Research Design
pubmed:year	2007
pubmed:articleTitle	Discussion of the "White Paper of the PhRMA Working Group on adaptive dose-ranging designs".
pubmed:affiliation	Center for Drug Evaluation and Research, US Food and Drug Administration, Rockvill 20857-0001, Maryland, USA. suejane.wang@fda.hhs.gov
pubmed:publicationType	Journal Article, Comment