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NEW YORK (GenomeWeb) – The US Food and Drug Administration's authorization last week of a 468-gene tumor profiling test puts into play several regulatory strategies that the agency has been mulling for some time, but it remains to be seen if other cancer centers and diagnostic companies with similar cancer panels will be willing to pursue the new pathway.

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Jul
23

This webinar will discuss how the Molecular Pathology Laboratory at the University of Oklahoma (OUMP) is using a new quality improvement model to support molecular testing of oncology patients.