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Counterpoint: Food and Drug Administration guidance for C-reactive protein assays: matching claims with performance

James V Callaghan1, Steven I Gutman

  • 1Office of In Vitro Diagnostic Device Evaluation and Safety, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA. james.callaghan@fda.hhs.gov

Clinical Chemistry
|June 27, 2006
PubMed
Abstract

No abstract available in PubMed .

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