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FDA perspective on the regulation of AI in health care and biomedicine

10.15.24 | JAMA Network

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About The Study: Strong oversight by the U.S. Food and Drug Administration (FDA) protects the long-term success of industries by focusing on evaluation to advance regulated technologies that improve health. The FDA will continue to play a central role in ensuring safe, effective, and trustworthy AI tools to improve the lives of patients and clinicians alike. However, all involved entities will need to attend to AI with the rigor this transformative technology merits.

Corresponding Author: To contact the corresponding author, Haider J. Warraich, MD, email haider.warraich@fda.hhs.gov .

To access the embargoed study: Visit our For The Media website at this link https://media.jamanetwork.com/

(doi:10.1001/jama.2024.21451)

Editor’s Note: Please see the article for additional information, including other authors, author contributions and affiliations, conflict of interest and financial disclosures, and funding and support.

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How to Cite This Article

APA:
JAMA Network. (2024, October 15). FDA perspective on the regulation of AI in health care and biomedicine. Brightsurf News. https://www.brightsurf.com/news/LVD92OYL/fda-perspective-on-the-regulation-of-ai-in-health-care-and-biomedicine.html
MLA:
"FDA perspective on the regulation of AI in health care and biomedicine." Brightsurf News, Oct. 15 2024, https://www.brightsurf.com/news/LVD92OYL/fda-perspective-on-the-regulation-of-ai-in-health-care-and-biomedicine.html.