U.S. Federal

The U.S. has few federal policies specifically addressing human genetic or assisted reproductive technologies. One exception is the 2008 Genetic Information Nondiscrimination Act (GINA), which prohibits the use of individuals’ genetic information in employment and health insurance. Another is the 1992 law requiring that fertility clinics provide standardized reports of success rates to the Centers for Disease Control.

Unlike scores of other countries with advanced biotech sectors, the U.S. has no federal laws regulating human reproductive cloning or heritable genome editing. However, the Food and Drug Administration (FDA) has asserted authority over these practices; the National Institutes of Health (NIH) makes decisions about research funding; and Congress has exerted some control over clinical applications of research involving human embryos through budget riders.

Biopolitical Times
The new Biden-Harris Administration faces a number of harrowing challenges in which science and technology policies will be critical.

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The genetic data will be added to an FBI database for violent criminals.
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The United States fertility market is growing very rapidly, and is projected to reach $15.4 billion in 2023, more than double...

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The president of one of the country’s largest at-home genetic testing companies has apologized to its users for failing to disclose that it was sharing DNA data with federal investigators.
In a grass field, a brown and white cow stares. On its right ear, there is an identification tag.

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A building, with a sign in front reading "US Department of Health and Human Services Federal Regulation Administration."

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Someone in a laboratory wears gloves on their hands, as they place a test tube filled with liquid into a centrifuge machine. Other laboratory equipment surrounds the room.

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A triangular warning sign posted against a wooden post. The sign is yellow, with a figurine that is slipping on water.

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Inside of a 23andMe packaging spit kit. On the right of the box, there is text that outlines instructions on how to submit a DNA sample. On the left, there are tools.

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A patient looks through an eye doctor's instrument, which covers their face almost completely.

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FDA Commissioner Scott Gottlieb stands behind a podium

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