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HR 2558 115th Congress House Health Administrative law and regulatory procedures Department of Health and Human Services Drug safety, medical device, and laboratory regulation Drug therapy Medical research Medical tests and diagnostic methods

Patient Safety and Toxicology Modernization Act of 2017

Introduced: May 19, 2017 See on congress.gov
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This bill died when the 115th Congress ended
It never became law before the 115th Congress (2017–2018) adjourned, and bills don't carry over to the next Congress. It would have to be reintroduced. You can still save it for reference, but it won't receive updates.
 Everywhere this bill has been 3 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
May 26, 2017
Referred to the Subcommittee on Health.
May 19, 2017
Referred to the House Committee on Energy and Commerce.
May 19, 2017
Introduced in House
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 Plain-English summary Congressional Research Service

Patient Safety and Toxicology Modernization Act of 2017

This bill requires the Food and Drug Administration to issue and periodically update guidance on: (1) novel tools for testing the toxicology and efficacy of medications, and (2) three-dimensional human tissue models.
What's happening now May 26, 2017

Referred to the Subcommittee on Health.

 Bill text 1 version

Source documents hosted by congress.gov.

 Committees of jurisdiction 2
 Cosponsors 1
All 1 Democratic 1
D
Peters, Scott H.
California · May 19, 2017
Cite this page click to expand
APA
U.S. Congress. (2026). H.R. 2558: Patient Safety and Toxicology Modernization Act of 2017. 115th Congress. Open America. https://openamerica.io/bill/115-HR-2558/
MLA
"H.R. 2558: Patient Safety and Toxicology Modernization Act of 2017." 115th Congress, 2026, Open America, https://openamerica.io/bill/115-HR-2558/.
Bluebook (legal)
H.R. 2558, 115th Cong. (2026), https://openamerica.io/bill/115-HR-2558/.
Markdown link
[H.R. 2558: Patient Safety and Toxicology Modernization Act of 2017](https://openamerica.io/bill/115-HR-2558/)
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