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Increased Transparency for Emergency Use Medical Products.

This act aims to increase the public availability of information regarding medical products authorized for emergency use. This will give citizens easier access to data on the safety and effectiveness of drugs and medical devices, enabling them to make more informed health decisions.
Key points
More information about medical products authorized for emergency use will be available on the Food and Drug Administration (FDA) website.
The act expands the scope of data that must be published, covering a wider range of applications and submissions for medical products.
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Additional Information
Emergency Use Transparency Act
Print number: S 3394
Sponsor: Sen. Hassan, Margaret Wood [D-NH]
Process start date: 2021-12-14