| Literature DB >> 17408233 |
Federico Goodsaid1, Felix Frueh.
Abstract
New biomarkers of safety and efficacy are becoming powerful tools in drug development. Their application can be accelerated if a consensus can be reached about their qualification for regulatory applications. This consensus requires a review structure within the US Food and Drug Administration (FDA) that can evaluate qualification data for these biomarkers and determine whether these biomarkers can be qualified. A pilot process and corresponding Biomarker Qualification Review Team have been developed to test how the FDA can work on biomarker qualification.Mesh:
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Year: 2007 PMID: 17408233 PMCID: PMC2751298 DOI: 10.1208/aapsj0901010
Source DB: PubMed Journal: AAPS J ISSN: 1550-7416 Impact factor: 4.009