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Understanding 21 CFR Part 882: Regulatory Standards for Neurological Devices
21 CFR Part 882Â outlines the regulatory requirements set forth by the U.S. Food and Drug Administration (FDA) for neurological devices.
Oct 22, 20243 min read
Elon Musk's Neuralink Secures FDA Approval for Human Trials
Elon Musk's Neuralink has achieved a major milestone with FDA authorization for its first human clinical trials.
Sep 26, 20242 min read
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