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HR 2244 115th Congress House Health Drug safety, medical device, and laboratory regulation Medical research Mental health User charges and fees

Patient Experience in Research Act of 2017

Introduced: April 28, 2017 See on congress.gov
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 5, 2017
Referred to the Subcommittee on Health.
Apr 28, 2017
Referred to the House Committee on Energy and Commerce.
Apr 28, 2017
Introduced in House
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 Plain-English summary Congressional Research Service

Patient Experience in Research Act of 2017

This bill requires the Food and Drug Administration to carry out a pilot project under which sponsors of new drugs or biological products agree to evaluate: (1) the distress experienced by patients in clinical trials for medications intended to treat a serious condition, and (2) the effects of providing support to distressed patients on the outcome of a clinical trial. The user fee is waived for new drug applications that include data from such an evaluation.
What's happening now May 5, 2017

Referred to the Subcommittee on Health.

 Bill text 1 version

Source documents hosted by congress.gov.

 Committees of jurisdiction 2
Cite this page click to expand
APA
U.S. Congress. (2026). H.R. 2244: Patient Experience in Research Act of 2017. 115th Congress. Open America. https://openamerica.io/bill/115-HR-2244/
MLA
"H.R. 2244: Patient Experience in Research Act of 2017." 115th Congress, 2026, Open America, https://openamerica.io/bill/115-HR-2244/.
Bluebook (legal)
H.R. 2244, 115th Cong. (2026), https://openamerica.io/bill/115-HR-2244/.
Markdown link
[H.R. 2244: Patient Experience in Research Act of 2017](https://openamerica.io/bill/115-HR-2244/)
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