US Senator Seeks Clarifications from FDA About Neuralink Inspection

Tuesday, 26 March 2024, 10:19

A U.S. lawmaker questions why the FDA permitted Neuralink to conduct human trials without prior inspection, raising concerns about the brain implant industry's regulations. The scrutiny on Elon Musk's Neuralink underscores the need for stricter oversight in the field of medical technology. The response from the FDA could shape the future of brain implant companies and their testing protocols.
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US Senator Seeks Clarifications from FDA About Neuralink Inspection

Exclusive – US lawmaker seeks answers on FDA inspection of Musk's Neuralink

By Marisa Taylor WASHINGTON - A U.S. lawmaker involved in health policy has asked the Food and Drug Administration why it did not inspect Elon Musk's Neuralink before allowing the brain implant company to test its device in humans. Reuters reported the senator's concerns over the FDA's regulatory process and the implications for innovative medical technologies.


This article was prepared using information from open sources in accordance with the principles of Ethical Policy. The editorial team is not responsible for absolute accuracy, as it relies on data from the sources referenced.


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