119 S 355
FDA Modernization Act 3.0
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Held at the desk.
2025-12-17
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Cosponsors (showing 9 of 9)
R · Schmitt, Eric (Missouri)I · King, Angus S., Jr. (Maine)R · Kennedy, John (Louisiana)D · Whitehouse, Sheldon (Rhode Island)R · Marshall, Roger (Kansas)D · Blumenthal, Richard (Connecticut)R · Paul, Rand (Kentucky)D · Luján, Ben Ray (New Mexico)D · Schiff, Adam B. (California)Federal Agencies on This Bill
Posts from federal agencies in the last 24 hours that match this bill's identifier or title keywords. Grouped by voice class — executive framing carries the administration's perspective; regulators speak to implementation; oversight bodies aim for neutrality. Read across, not just within, a single voice class.
Regulators (rule-making and recall language)
Output from FDA, CDC, EPA, SEC, FCC, FTC, NHTSA and similar bodies. These are typically issuing rules under existing statutory authority — useful signal for which provisions of a bill would actually be implemented and where.
Modernizing Reactor Licensing, Safety Oversight, and Siting Practices; Correction
The U.S. Nuclear Regulatory Commission (NRC) is correcting a notice published in the Federal Register on July 16, 2026, regarding the modernization of reactor licensing, safety oversight, and siting practices to address sections 5(f), 5(h), and 5(i) of Executive Order 14300, and
Read on federalregister.gov →Markets vs Bill
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APA
Apprised.news. (n.d.). 119 S 355: FDA Modernization Act 3.0. Retrieved 2026-07-28, from https://apprised.news/bill/119s355
MLA
"119 S 355: FDA Modernization Act 3.0." Apprised.news. Web. 2026-07-28. <https://apprised.news/bill/119s355>.
Chicago
"119 S 355: FDA Modernization Act 3.0." Apprised.news. Accessed 2026-07-28. https://apprised.news/bill/119s355.
BibTeX
@misc{apprised_119_s_355_fda_modernization_act_3_0,
title = {119 S 355: FDA Modernization Act 3.0},
publisher = {Apprised.news},
url = {https://apprised.news/bill/119s355},
note = {Accessed 2026-07-28}
}