Daniel Yarbrough, Ph.D.

Daniel Yarbrough, Ph.D.

Knobbe Martens

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FDA Approval of 23andMe Genomic Test Shows the Way for Direct-to-Consumer Diagnostics

On April 6, 2017 the FDA Center for Devices and Radiological Health formally approved 23andMe’s Personal Genome Services Test as a Class II Medical Device. Approved tests include assessment of an individual’s genetic risk of...more

4/21/2017  /  23andMe , FDA Approval , Food and Drug Administration (FDA) , Human Genome Project , Medical Devices
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