A bill to eliminate requirements to undertake duplicative clinical testing of new pharmaceutical drugs, vaccines, biological products, or medical devices, when such duplication is inconsistent with relevant ethical norms.
The bill’s titles are written by its sponsor.
Sponsor and status
Sponsor. Senator for Vermont. Independent.
Last Updated: Aug 2, 2012
Length: 7 pages
Aug 2, 2012
112th Congress, 2011–2013
Died in a previous Congress
This bill was introduced on August 2, 2012, in a previous session of Congress, but was not enacted.
Sep 29, 2010
Earlier Version — Introduced
This activity took place on a related bill, S. 3921 (111th).
Aug 2, 2012
Bills and resolutions are referred to committees which debate the bill before possibly sending it on to the whole chamber.
S. 3506 (112th) 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 112th Congress, which met from Jan 5, 2011 to Jan 3, 2013. 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). S. 3506 — 112th Congress: Ethical Pathway Act of 2012. Retrieved from https://www.govtrack.us/congress/bills/112/s3506
“S. 3506 — 112th Congress: Ethical Pathway Act of 2012.” www.GovTrack.us. 2012. April 20, 2018 <https://www.govtrack.us/congress/bills/112/s3506>
|title=S. 3506 (112th)
|accessdate=April 20, 2018
|author=112th Congress (2012)
|date=August 2, 2012
|quote=Ethical Pathway Act of 2012
Where is this information from?
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