By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – Molecular diagnostics firm OvaGene on Monday announced its laboratory has received Clinical Laboratory Improvement Act certification, making it fully licensed to receive patient clinical specimens from gynecological oncologists from most of the US.

Based in Irvine, Calif., OvaGene develops gene-based diagnostics for gynecological cancer.

Frank Kiesner, chairman and CEO of OvaGene, said the certification marked a milestone for the company.

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