To amend the Federal Food, Drug, and Cosmetic Act to promote the use of adaptive trial designs, Bayesian methods, and other innovative statistical methods in clinical protocols for drugs, biological products, and devices, and with respect to the requirement to conduct postapproval studies and clinical trials, and for other purposes.
The bill’s titles are written by its sponsor.
Sponsor and status
Sponsor. Representative for New York's 27th congressional district. Republican.
Last Updated: Feb 25, 2015
Length: 7 pages
Feb 25, 2015
114th Congress, 2015–2017
Died in a previous Congress
This bill was introduced on February 25, 2015, in a previous session of Congress, but was not enacted.
What stakeholders are saying
Feb 25, 2015
Bills and resolutions are referred to committees which debate the bill before possibly sending it on to the whole chamber.
H.R. 1066 (114th) was a bill in the United States Congress.
A bill must be passed by both the House and Senate in identical form and then be signed by the President to become law.
This bill was introduced in the 114th Congress, which met from Jan 6, 2015 to Jan 3, 2017. Legislation not enacted by the end of a Congress is cleared from the books.
How to cite this information.
We recommend the following MLA-formatted citation when using the information you see here in academic work:
Civic Impulse. (2018). H.R. 1066 — 114th Congress: Clinical Trials Modernization Act of 2015. Retrieved from https://www.govtrack.us/congress/bills/114/hr1066
“H.R. 1066 — 114th Congress: Clinical Trials Modernization Act of 2015.” www.GovTrack.us. 2015. February 24, 2018 <https://www.govtrack.us/congress/bills/114/hr1066>
|title=H.R. 1066 (114th)
|accessdate=February 24, 2018
|author=114th Congress (2015)
|date=February 25, 2015
|quote=Clinical Trials Modernization Act of 2015
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