FDA gives nod to 23andMe for no-prescription breast cancer gene testing

17:43 EST 6 Mar 2018 | MedCity News

Red seal and imprint "FDA APPROVED" on white surface. FDA - Food and Drug Administration is a federal agency of the United States Department of Health and Human Services.

The Food and Drug Administration has granted 23andMe the first-ever authorization for direct-to-consumer genetic testing for cancer risk without a prescription.

Original Article: FDA gives nod to 23andMe for no-prescription breast cancer gene testing

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